Ladies and gentlemen, thank you for standing by, and welcome to Nanox third quarter 2022 earnings conference call. At this time, all participants are on a listen-only mode. After the speaker presentation, there will be a question and answer session. To ask a question during this session, you will need to press star one one on your telephone keypad. Please be advised that today's conference may be recorded. I would now like to hand the conference over to your speaker host, Mike Cavanaugh of Investor Relations. Please go ahead.
Good morning, and thank you for joining us today. Earlier today, Nano-X Imaging Ltd. released its financial results for the quarter ended September 30, 2022. The release is currently available on the investors section of the company's website. Erez Meltzer, Chief Executive Officer, and Ran Daniel, Chief Financial Officer, will host this morning's call. Before we get started, I would like to remind everyone that management will be making statements during this call that include forward-looking statements regarding the company's financial results, research and development, manufacturing and commercialization activities, regulatory process operations, and other matters. These statements are subject to risks, uncertainties and assumptions that are based on management's current expectations as of today and may not be updated in the future. Therefore, these statements should not be relied upon as representing the company's views as of any subsequent date.
Factors that may cause such a difference include, but are not limited to those described in the company's filings with the Securities and Exchange Commission. We will also refer to certain non-GAAP financial measures to provide additional information to investors. A reconciliation of the non-GAAP to GAAP measures is provided with our press release, with the primary differences being amortization of intangible assets, share-based compensation, secondary offering expenses, goodwill impairment, change in obligation in connection with acquisitions and legal fees in connection with class action litigation and the SEC inquiry. I'd now like to turn the call over to Erez Meltzer.
Thank you, Mike, and thank you all for joining the call today. Reporting on our third quarter of 2022, I'm proud of the results our team has been able to deliver as we continue to advance our commercialization of the Nanox.ARC system. As in our last call, I will give an overview of our recent achievements, and we'll share our outlook for the rest of 2022. Before turning the call over to Ran Daniel, our CFO, to review our financial results in detail, we will then open the call up to questions. I'm pleased with the progress our team made during the quarter, which, as most of you know, include our 510(k) submission to the FDA for our multi-source Nanox.ARC system at the end of September, and which is now under FDA review.
I'm very proud of the hard work behind the scenes by our regulatory product and other teams to absorb the continuous feedback from our Q-Submission process and incorporated it into the recent submission. We do not have any insights into the timing of the FDA's response. In other regulatory news, we continue to pursue CE mark approval in the European Union, and I'm happy to report that we have engaged with BSI, the notified body with whom we will work during this process. We look forward to providing updates to you as the process advances in the coming months. I'd like to take a few minutes now to discuss our progress toward commercialization of the multi-source Nanox.ARC system. It remains our goal to begin to deploy the multi-source Nanox.ARC system in 2022, and we continue to push toward the goal.
We continue to advance the process toward deployment of the multi-source Nanox.ARC in Nigeria, subject to regulatory approval as we recently received an import license. We intend to ship the first system and begin training soon as we aim to secure regulatory approval. Globally, we have total of 6,850 pre-ordered units. We believe that once we begin to deploy the multi-source Nanox.ARC in Nigeria and in other early adopting countries, health system hospitals and distributors will see the service that the Nanox.ARC provides. Clinical updates. We have received the Helsinki permits to conduct clinical trials in Israel using our multi-source Nano Trial system. We anticipate that the results of these trials will generate clinical sample images of multiple body organs during the fourth quarter of 2022. Now turning to our AI and teleradiology business segments.
We continue to see revenue from these important business segments. I'm happy to report that during the third quarter of 2022, we signed 9 new client agreements for teleradiology services, and we continue to see revenue growth in these services driven by new client additions as well as organic growth from existing clients. These businesses generated top line revenue of $2.4 million in the third quarter of 2022, compared to $2.2 million in the second quarter of 2022. Ran will review the financials in more detail, but these revenues continue to demonstrate the viability and utility of these additional services to the healthcare system, which services are intended to be part of the fully integrated multi-source Nanox Arc system upon deployment and an integral part of our ecosystem and end-to-end solution.
Before I turn the call over to Ran, I'd like to remind everyone that we will be hosting a multi-source Nanox.ARC demonstration broadcast with a live audience in Neve Ilan on Wednesday, November 16 at 9:30 A.M. Eastern Time. Due to the capacity limitation, we invite you to attend virtually. You can find the link for registration on our website. I want to thank our investors for their continued support of our vision to help make medical imaging accessible throughout the world. I'm very happy with the progress we made this quarter, and we look forward to meeting additional milestones as we move toward large-scale commercialization. With that, I'd like to turn the call over to Ran Daniel, Chief Financial Officer, to review our financial results.
Thank you, Erez. We reported a GAAP net loss for the third quarter of 2022 of $19.1 million, compared with a net loss of $13.5 million in the third quarter of 2021, which increase was largely due to the consolidations of Nanox.AI and USARAD with the company since the fourth quarter of 2021, an increase in our research and development expenses, an increase in our general administrative expenses, which was mitigated by a decrease in our sales and marketing expenses, and a $1.0 million expense due to a change in our obligation in connection of acquisitions. Revenues for the third quarter of 2022 was $2.4 million, and gross loss was $1.4 million.
Revenue from teleradiology services for the same period was $0.3 million, with a gross profit of $0.6 million on a GAAP basis and a gross profit of $1.2 million on a non-GAAP basis, which represents a gross profit margins of approximately 49.4%. The increase in the company's revenue and the gross profit margins in the third quarter of 2022 is due to revenues from a data monetization project with a total revenue of $0.3 million. Revenue from licensing of AI applications for the same period was $0.1 million, with a gross loss of $2.1 million on a GAAP basis and $0.0 million on a non-GAAP basis.
Research and development expenses for the third quarter of 2022 were $6.1 million, as compared to $3.7 million for the comparable period in 2021. The increase in our research and development expenses was mainly due to the consolidation of Nanox.AI with the company, as well as due to the development of the multi-source Nanox.ARC and the Nanox.CLOUD and share-based compensation. Sales and marketing expenses for the third quarter of 2022 were $0.7 million, as compared to $1.5 million for the comparable period in 2021. The decrease was mainly due to a decrease in cost of labor and share-based compensation. General and administrative expenses for the third quarter of 2022 were $10.6 million, as compared to $8.2 million for the comparable period in 2021.
The increase was due largely to the consolidation of Nanox.AI and USARAD with the company since the fourth quarter of 2021, an increase in the company's head count and the overall organizational infrastructure and an increase in the company's legal fees due to the U.S. Securities and Exchange Commission inquiry and class action litigation, as described in the company's Form 6-K filed today and Form 20-F for the year ended December 31, 2021, filed on May 2, 2022. Change in obligations in connection with acquisitions was $1.0 million as compared to none in the comparable period due to the increase in the company's contingent earnout liability.
The non-GAAP net loss for the third quarter of 2022 was $8.1 million, compared to a non-GAAP net loss of $8.4 million for the same period in 2021. A reconciliation between GAAP net loss and non-GAAP net loss for the third quarter of 2022 and 2021 is provided in the financial results that are part of the press release that we issued this morning. Turning to our balance sheet. As of September 30, 2022, we had cash equivalents and marketable securities of approximately $117.1 million, and we had $3.5 million in loans from banks. We entered the quarter with property and equipment net of $44.1 million, compared with $37.4 million as of December 31, 2021.
The increase is largely due to the purchasings of long-lived items for our multi-source systems and machinery and equipment for our fabrication facility in South Korea. As of September 30, 2022, we had approximately 52.3 million shares outstanding as opposed to 51.8 million shares outstanding as of December 31, 2021. The increase was mainly due to the exercise of stock options. With that, I will hand the call back over to Erez.
Thank you, Ran, for the financial update. Once again, thank you all for joining us today. I feel very good about Nanox results in the third quarter as CEO, but all of us recognize there is more to do. We hope to provide additional updates in the coming weeks and months. With that, I'd like to now open the call for questions. Operator, please begin the Q&A session.
Thank you. Ladies and gentlemen, to ask a question, you will need to press star one one on your telephone keypad. Please stand by while we compile the Q&A roster. Our first question coming from the line of Jeffrey Cohen with Ladenburg. You'll un-mute yourself then.
Hello, Erez and Ran. How are you?
Great. You, Jeff?
Just fine. A few questions for you. I guess firstly, as far as Nigeria and units that may be available for placement, could you give us a sense of manufactured ARC units as they stand at the moment?
In terms of manufacturing, we are, as we say, in the process. We have all the materials which is available. We are making actually, we work hand in hand with the regulatory approval. Once we get all the paperwork, we can start to ship the units. It goes the same with the other countries, when we get all the regulatory approvals. We have to just to complete the answer about Nigeria. The next step is send the first unit for demonstration. The demo center is ready already over there, and then to engage with those customers who are expecting to get the machines to do the training.
As you know, we've indicated the work that we do with BVGH for the deployment and the training in Nigeria. That's the process that we do.
Can you give us a sense of the size of the order over the coming year, specific to Nigeria?
As you know, and I'm going to stick to it, until further or later or future other indications, we haven't given numbers so far. The main reason, of course, was regulation. We haven't given numbers so far, and we may change it in the future.
Got it. Okay. Jumping over to the teleradiology, could you give us a sense of number of accounts and/or account growth and utilization trends and utilization growth?
Okay. Ran, would you like to address this question?
Yes. Jeffrey, we had an additional nine accounts this quarter. The total accounts is approximately 400 as of now. You can calculate yourself the growth rate of it.
Basically, you see the numbers in terms of the revenues, the growth rates. We are still waiting for all the approvals and licenses and accreditation that we are waiting always when we sign, there is a gap between the time that we can start do the readings. Right now, in terms of the customers, as always, we have the sort of, I would say, 60/40 or 70/30, where a few customers are generating pretty much of the, I would say majority, at least 60% of the revenues. Right now, what we see is a lot of growth in those that have been with us for quite some time, and we see the future as well.
Okay, got it. Could you talk about the $2 million of goodwill impairment for the quarter? Is there more to impair? I can see the goodwill number, but would you anticipate any more breakdowns of that goodwill number for the balance of the year, or give us a sense of what was written down for the third quarter?
Yes. Just to complete my answer before, as to the new accounts there, radiologist accounts. It takes us, as Erez said, two to three months to go through the credentialing process once we get a new client. That's just to complete my other answer. As for the goodwill, the goodwill is really like the goodwill impairment comes from a few factors. The two main ones are, first, you know, a change in the discount rate that we're using. You know, as long as the Federal Reserve continues to increase the rates, we should expect to at least be required to examine if an impairment is needed, and that's what we're doing on a quarterly basis.
This specific quarter, there was no impairment, but there was indication that the impairment is needed, so we had to go through the whole process. As for your question, as for the third quarter-
Impairment is, there's no impairment expense, but we had to go through the whole process. As for the fourth quarter, you can also consider the fact that, you know, we'll have to consider our estimates for the 2023 and going forward, coupled with any change that will be in the discount rates that will be done by the Federal Reserve. Now, you can imagine, by the way, that once we start the deployment of the Arc, obviously all the teleradiology services will be expanded and grow.
Got it. Finally for us, just review where things stand at the FDA as far as the permutations that we should expect going forward. We do anticipate that obviously a clearance would be one option. The second would be that they would be back with additional questions. What are the few permutations that we could see?
Okay. The one thing that I don't bet or indicate is the timing of the process from the FDA. We saw it in the last three years, and I think the whole world, the whole business world, but we see it as we see it right now. What we are saying that we have done the utmost or everything that we could in order to increase the likelihood of the clearance from the FDA.
Having said that, we spoke about it and we have emphasized it, that this year Nanox has changed a little bit its regulatory strategy from the single step FDA submission process to a stepwise approach using Q-Submission path for questions and answers with the FDA team prior to the 510(k) submission. Frankly speaking, we intend to continue to use this dialogue with the FDA as we develop the next generation of the Nanox.ARC system, as well as the future products that Nanox will generate.
Perfect. Okay, we look forward to next week. Thanks for taking our questions here, Erez.
Thank you. Thank you.
Thank you. One moment before our next question. Now, our next question in queue coming from the line of Ross Osborn with Cantor Fitzgerald. Your line is open.
Hi, hope everyone's doing well. Congrats on the progress.
Hi, how are you?
I'm well, thank you.
Okay. How are you?
Starting off, is there any update on the Ghana contract? I know you noted a special approval process on last quarter's call. If you could provide a little bit more color just on what the regulatory environment is there and kind of where you stand in timing.
You asked about the Ghana deployment?
Yes, that's correct.
You know, we did it now up until now, and we'll do it in the future, that as soon as we have information which is needed to be shared with the public, we'll do. We signed, as you know, the agreement. We're waiting for the regulatory processes. Once we get the clearance, as we did now with Nigeria, or the approval, then we'll release it. By the way, in the meantime, of course, as we do with any other countries, we do all the preparations.
We're meeting with the customers, doing initial trainings, checking all the availability of the internet and telecommunication infrastructure, try to see what is needed in terms of the training itself, et cetera. Since we have already said that we expect that the initial deployment of the Nanox.ARC at scale, as we say, to be done in outside of the U.S., then basically that's where we're doing all the standalone 3D digital tomosynthesis units. Our approach is right now to do the deployment in the U.S. only in the next step. We'll inform when we actually get the dialogue with the FDA and as soon as we can get it.
We are making all the preparation even in the countries that will require the FDA, namely meeting distributors, getting to know better the customers, do all the preparation of the regulatory processes, et cetera. Once we get the clearance, then we can actually move fast forward.
Okay. Sounds great. I guess just one more on the Ghana contract. I know you disclosed 350 units. Are you able to provide us with the minimum annual fee and then, if there is a letter of credit, associated with the contract?
There is always the difference between able and will. The answer is that as soon as we have something to say, we will say.
Okay. Fair enough. I guess looking ahead of deployment, do you expect for the scans to be read in Nigeria, or would those be outsourced to Nanox? If it is the latter, you know, do you have radiologists in place and are those radiologists, you know, financially motivated to read the scans?
Right now, based on everything that we know right now, which may change in the future, but based on the studies and the groundwork that within Nigeria, it will be both.
Okay, great. Thank you for taking my questions.
Thank you, Ross.
One moment please for our next question. Our next question in queue coming from the line of Suraj Kalia with Oppenheimer. Your line is open.
Good morning, Erez, Ran. How are you?
Good. How are you, Suraj?
Good morning.
I'm doing well. Hey, so, Erez, bunch of questions. Erez, can you give us this, as you look for commercialization, let's say to begin off in Nigeria, how would the workflow for these products look? i.e., what happens in Israel? What happens in Korea, especially your manufacturing facility? What happens in Japan, ceramic or glass tube? Just kind of walk us through how the workflow is expected to happen.
You know, it's interesting and it's funny, but actually what you are asking for is a demo next week. On the ARC day, you will see the whole flow. As we have explained in the past, the chips are being manufactured in Korea. The tubes are being installed in Korea, and we are planning to do more of it in the future from other suppliers. All the integration and the assembly is being done currently in Israel and in the future, as we said in the prospectus and the 20-F, part of it will be done outside of Israel.
The system is fully installed and assembled in Israel, and when it ships, it ships actually a few in a box and it ships to the place that they are going to be deployed. In Nigeria, you asked specifically about Nigeria, but it will be the same in other countries. We are doing the installation, the connection to the network, to the system, sometimes even to the PACS system in the future. We do all the training of the operators. We do all the training of the maintenance on site. We do the training of the radiologist on premise. We have a demo center. We will have a demo center in every country that we're going to deploy.
Right now in Nigeria, we have already the demo center ready to install the first unit. What else? Of course, the maintenance afterwards and the initial operating of the units will be on the ground. We work with partners. In Nigeria, we're going to explore the work that we're planning to do with other partners as well. It's not be only one, but it will be a few of them. We have already engaged ourselves in a dialogue with the customers and hospitals in Nigeria, by the way, in other countries as well. That's actually. I hope that I addressed in detail the answer to your question.
Fair enough. Erez, I presume the Nigeria configuration is the same as the U.S. configuration?
It's a good question. Hopefully, yes. But we don't know what will be. We hope that the FDA will approve the same as that we have intended to use. I hope that no changes will take place. Basically, that's the answer.
Got it. Erez, finally, the 6,800 or so confirmed pre-orders that you talked about, how confident are you with these contracts in their ability to fulfill, you know, your ability to enforce? Because a lot of them, you know, our recollection is, you know, they're at least a few years old and have not gone through validation testing. Any additional color would be greatly appreciated. Gentlemen, thank you for taking my questions.
Okay. I think that I'm more than 40 years in business, 40, and more than 35 years as a CEO. The one thing I've learned in business is that basically you are confident in the deal and the transaction once the money is in your bank. In this specific place when the money from each one of them will be in our bank account. This is in terms of confidence. But having said that, it all depends on the clearance processes and approvals and regulations in any one of the place. We are in continuous dialogue with these business entities that we signed the agreement with.
A few of them, by the way, are coming from time to time to Israel to see the progress and to do some training and to get to know better the system, the product and the intended use. That's basically the answer.
Thank you.
Thank you, one moment please, for our next question in queue. Our next question in queue coming from the line of Rahul Rakhit with LifeSci Capital. Your line is open .
Hey, guys. Thanks for taking the questions. I was just wondering if you could touch a little bit on the initial utilization levels at Northwell and Spectrum Health. Maybe help us better understand how to think about the revenue generation from, you know, these IDNs moving forward.
First of all, we have not indicated that specifically from each one of the IDNs. I will add or say a couple of things. The discussion with one of the IDNs that we have already installed and received the money last year, the agreement or the extension of the agreement for next year is with much higher revenues coming from the IDN. In terms of Northwell, this is a continuous dialogue. We have already, I think, few hospitals that were already installed as part of the project. Northwell, I would say, is more than just an IDN. They are kind of strategic IDN that we work with that we've jointly developed some applications.
We jointly develop some business models and intended use of the AI application. They are planning to adapt and install all the applications that we have. As you know, we have two in place, and a few others are coming soon. Last but not least, we are in the final process of developing the future business model that will help us to indicate what is the value that we bring to the IDN, to the insurance company, to the pharmaceutical company, and tailor-made to each one of them, like, what would be the best model in order for our benefits to grow the business, but also that they will enjoy from the added value of our services.
Got it. Okay. Thank you. Thank you for that.
Rahul, just one more sentence. We have not been, as Erez said, we have not indicated the amount of revenue that we generated or going to generate from those two projects. Nevertheless, you have to bear in mind, those are the two projects that we have in the health populations area.
Got it. No, I appreciate that. Thank you.
You're welcome.
Just one more from me. Can you tell us a little bit more about the clinical trials that you intend to conduct in Israel? You know, can you provide any color on trial design or what images specifically you guys are focusing on initially? How you intend to leverage that data moving forward? Thank you for taking the questions.
We'll update as soon as we complete getting the samples. The one thing that we've indicated that we've received the Helsinki permit to conduct the clinical trials in one of the leading hospitals. The system is already installed there. The X-ray room is already installed there. We anticipate that the results of these trials will, for us, will generate sample of images of multiple body organs during this quarter, the fourth quarter of 2022. I do hope, believe, and anticipate that in the next earnings call, we'll have more to share about it.
Thank you. I am opening now for the questions at this time. I would now like to turn the call back over to Mr. Meltzer for any closing remarks.
Thank you all for taking the time to be with us. For those of you who have actually more interest in what we have to show and indicate, I hope that next week will be good for these people that would like to see. I thank you, all the investors, for being with us, and we hope to fulfill our promises, the promises that we made to make everything happen and to really change the world in what we're doing.
Ladies and gentlemen, that does end our conference for today. Thank you for your participation. You may now disconnect. Good day.