Fidia S.p.A. (BIT: FDA)

Italy flag Italy · Delayed Price · Currency is EUR
0.0408
-0.0030 (-6.85%)
Dec 20, 2024, 5:35 PM CET
-96.39%
Market Cap 1.27M
Revenue (ttm) 29.17M
Net Income (ttm) -6.44M
Shares Out 31.09M
EPS (ttm) -0.44
PE Ratio n/a
Forward PE n/a
Dividend n/a
Ex-Dividend Date n/a
Volume 3,705,120
Open 0.0438
Previous Close 0.0438
Day's Range 0.0400 - 0.0448
52-Week Range 0.0398 - 1.1100
Beta 0.07
Analysts n/a
Price Target n/a
Earnings Date Mar 17, 2025

About Fidia

Fidia S.p.A., together with its subsidiaries, designs, manufactures, and sells high speed milling systems, numerical controls, milling heads, and software systems. Its accessories comprise HMS, a device for measuring and compensating geometric error on continuous or indexed bi-rotary heads and roto-tilting tables; TMSC, a device to measure length and diameter of the tool, as well as to check the shape; K5 tracer, a solution to perform continuous scanning of 3D surfaces; pushbutton panels; XPower digital drives for axis and spindle movement; and... [Read more]

Sector Industrials
Founded 1974
Employees 193
Stock Exchange Borsa Italiana
Ticker Symbol FDA
Full Company Profile

Financial Performance

Financial Statements

News

Popular Dog Arthritis Medication May Have Severe Side Effects, FDA Says

The drug has been associated with severe side effects such as seizures and muscle control loss, with over 3,600 adverse health reactions reported.

9 hours ago - NDTV

FDA approves Alhemo® injection as once-daily prophylactic treatment to prevent or reduce the frequency of bleeding episodes for adults and children 12 years of age and older with hemophilia A or B with inhibitors

FDA approval is based on data from the pivotal phase 3 trial (explorer7) establishing the safety and efficacy of Alhemo ® for daily prevention of bleeds in adults and pediatric patients 12 years of ag...

16 hours ago - Benzinga

Eli Lilly's Obesity Drug Wins Approval In Sleep Apnea; Will ResMed Dive?

Eli Lilly gained FDA approval late Friday for its weight-loss drug, Zepbound, as a treatment for obstructive sleep apnea.

17 hours ago - Investor's Business Daily

Market Today: Qualcomm's Legal Victory and Pfizer's FDA Approval Highlight Key Developments

Market Today: Qualcomm's Legal Victory and Pfizer's FDA Approval Highlight Key Developments

18 hours ago - GuruFocus

FDA Approves Eli Lilly's Zepbound for Obstructive Sleep Apnea in Adults with Obesity

FDA Approves Eli Lilly's Zepbound for Obstructive Sleep Apnea in Adults with Obesity

18 hours ago - GuruFocus

FDA approves weight loss drug Zepbound for sleep apnea

Zepbound, Eli Lilly’s weight loss drug, can now be used to treat obstructive sleep apnea in adults with obesity, the FDA said.

18 hours ago - NBC News

FDA approves Eli Lilly's weight loss drug Zepbound for sleep apnea, expanding use in U.S.

The agency's decision expands the use of Zepbound and could potentially pave the way for Eli Lilly to gain broader insurance coverage for the treatment.

18 hours ago - CNBC

FDA approves Zepbound® (tirzepatide) as the first and only prescription medicine for moderate-to-severe obstructive sleep apnea in adults with obesity

Averaging up to 20% of weight loss, adults taking Zepbound had at least 25 fewer breathing interruptions each hour as they slept Up to 50% of adults taking Zepbound no longer had symptoms associated w...

19 hours ago - Benzinga

Vertex Pharmaceuticals (VRTX) Gains FDA Approval for ALYFTREK™

Vertex Pharmaceuticals (VRTX) Gains FDA Approval for ALYFTREK™

19 hours ago - GuruFocus

Vertex Pharmaceuticals Inc (VRTX) Announces FDA Approval of ALYFTREK for Cystic Fibrosis Treatment

Vertex Pharmaceuticals Inc (VRTX) Announces FDA Approval of ALYFTREK for Cystic Fibrosis Treatment

19 hours ago - GuruFocus

Eggs now qualify as ‘healthy’ food, FDA says: Here’s why

The U.S. Food and Drug Administration (FDA) now classifies eggs as a “healthy, nutrient-dense" food, according to a new proposed rule. Registered dietitians react to the change.

20 hours ago - Fox News

Pfizer Inc (PFE) Gains FDA Approval for New Colorectal Cancer Treatment

Pfizer Inc (PFE) Gains FDA Approval for New Colorectal Cancer Treatment

20 hours ago - GuruFocus

Rhythm Pharmaceuticals Inc (RYTM) Expands FDA Approval for IMCIVREE® to Treat Young Children ...

Rhythm Pharmaceuticals Inc (RYTM) Expands FDA Approval for IMCIVREE® to Treat Young Children with Rare Obesity Disorders

20 hours ago - GuruFocus

Catalyst Watch: Labor pains for Amazon & Starbucks, Nasdaq call-up for MicroStrategy and Pony AI ratings

Next week's stock market events include earnings reports, index shuffles, FDA action dates, and the Wall Street Gambit event.

20 hours ago - Seeking Alpha

Dow Surges Over 600 Points, Gold Jumps 1.5%

U.S. stocks traded higher toward the end of trading, with the Dow Jones index jumping more than 600 points on Friday. The Dow traded up 1.55% to 43,000.53 while the NASDAQ rose 1.65% to 19,693.06. The...

20 hours ago - Benzinga

FDA recognises tea as a ‘healthy’ beverage

Kolkata: The Indian Tea Association (ITA) on Friday announced that the US Food and Drug Administration (FDA) has issued a final rule updating the "hea.

20 hours ago - The Times of India

Merit Medical gets FDA approval for WRAPSODY dialysis device

Merit Medical Systems (MMSI) has received FDA approval for its WRAPSODY Cell-Impermeable Endoprosthesis device for the treatment of dialysis patients. Read more here.

22 hours ago - Seeking Alpha

Nasdaq Jumps Over 300 Points, Novo Nordisk Shares Spike Higher

U.S. stocks traded higher midway through trading, with the Nasdaq Composite jumping more than 300 points on Friday. The Dow traded up 1.82% to 43,111.11 while the NASDAQ rose 1.77% to 19,714.27. The S...

22 hours ago - Benzinga

Mission Produce, Nvidia, Humacyte, BlackBerry And Other Big Stocks Moving Higher On Friday

U.S. stocks were higher, with the Dow Jones index gaining over 300 points on Friday. Shares of Mission Produce, Inc . (NASDAQ: AVO) rose sharply during today's session after the company reported bett...

1 day ago - Benzinga

Why Is Bioengineered Human Tissue-Focused Humacyte Stock Surging On Friday?

On Thursday, the FDA granted full approval to Humacyte, Inc.’s (NASDAQ: HUMA) Symvess (acellular tissue-engineered vessel-tyod) use in adults as a vascular conduit for extremity arterial injury when ...

1 day ago - Benzinga

Humacyte surges on FDA approval for Symvess vascular repair product

Humacyte (HUMA) stock climbs as FDA approves Symvess, its implantable vascular conduit for arterial injury. Read more here.

1 day ago - Seeking Alpha