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

Italy flag Italy · Delayed Price · Currency is EUR
0.0064
0.00 (0.00%)
Jun 10, 2026, 5:35 PM CET
Market Cap3.20M -22.2%
Revenue (ttm)32.40M +70.0%
Net Income1.04M
EPS0.00
Shares Out 499.41M
PE Ratio2.13
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volume6,681,620
Open0.0066
Previous Close0.0064
Day's Range0.0062 - 0.0066
52-Week Range0.0030 - 0.6100
Beta0.39
Analystsn/a
Price Targetn/a
Earnings DateMay 29, 2026

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. The company offers 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; pushbutton panels; XPower digital drives for axis and spindle movement; and I/O Line input/output modules. It also provides software solutions include... [Read more]

Founded 1974
Employees 140
Stock Exchange Borsa Italiana
Ticker Symbol FDA
Full Company Profile

Financial Performance

Financial Statements

News

Alterity Aligns With FDA On Phase 3 Design For ATH434 In Treating Multiple System Atrophy

(RTTNews) - Alterity Therapeutics (ATHE), a biotechnology company, on Tuesday reported achieving alignment with the U.S. Food and Drug Administration (FDA) on the planned Phase 3 trial for ATH434 in t...

8 hours ago - Nasdaq

Cellectis (CLLS) Receives FDA RMAT Designation for CAR-T Therapy, Shares Rise

Cellectis (CLLS) Receives FDA RMAT Designation for CAR-T Therapy, Shares Rise

10 hours ago - GuruFocus

FDA Accepts Takeda's SBLA For ENTYVIO IV In Pediatric UC And Crohn's Disease; PDUFA Set In Q1,2027

(RTTNews) - Takeda Pharmaceutical Company Ltd. (TAK) announced that the U.S. Food and Drug Administration (FDA) has accepted its supplemental Biologics License Application or sBLA for intravenous ENTY...

11 hours ago - Nasdaq

Lilly Receives FDA Nod For EBGLYSS Eight-Week Subcutaneous Maintenance Dose In Atopic Dermatitis

(RTTNews) - Eli Lilly and Company (LLY) announced that the U.S. Food and Drug Administration (FDA) has approved an every-eight-week maintenance dosing schedule for EBGLYSS or lebrikizumab-lbkz (250 mg...

12 hours ago - Nasdaq

Eli Lilly (LLY) Receives FDA Nod for Ebglyss Maintenance Regimen

Eli Lilly (LLY) Receives FDA Nod for Ebglyss Maintenance Regimen

17 hours ago - GuruFocus

The FDA just glowed up your sunscreen — by approving a popular ingredient in European and Asian formulas

For decades, US sunscreens lagged behind formulas in Europe and Asia. Now, a new FDA-approved ingredient is helping America catch up.

18 hours ago - Business Insider

Takeda (TAK) Gains FDA Review for Pediatric Ulcerative Colitis Treatment

Takeda (TAK) Gains FDA Review for Pediatric Ulcerative Colitis Treatment

19 hours ago - GuruFocus

FDA cracks down on illegal drug trade, stock worth about ₹25 lakh seized from Pune and Kolhapur

FDA seized illegal medicines worth ₹24.81 lakh in Pune and Kolhapur, including unlicensed antibiotic stocks and improperly promoted Schedule H drugs, officials said.

22 hours ago - The Times of India

Birthday cake turns into nightmare as toddler swallows hidden metal pins

Toddler in Thane swallows metal pins hidden in cake decorations; X-ray confirms pins in intestine, passed naturally. Family seeks action under FDA, consumer law.

23 hours ago - The Times of India

Medline Industries Faces Regulatory Crisis Amid FDA Warnings (MDLN)

Medline Industries Faces Regulatory Crisis Amid FDA Warnings (MDLN)

1 day ago - GuruFocus

FDA approves first new sunscreen ingredient in more than 25 years

Federal health regulators have signed off on the first new sunscreen ingredient for the U.S. market in more than 25 years.

1 day ago - Associated Press

FDA Approves the First New Sunscreen Ingredient in 20 Years

Bemotrizinol is a powerful, broad-spectrum blocker of dangerous rays that has been used in Europe for years.

1 day ago - TIME

FDA allows popular sunscreen ingredient long used in Europe and Asia

The Food and Drug Administration on Tuesday expanded its list of allowed sunscreen ingredients to include the chemical compound bemotrizinol.

1 day ago - NBC News

Disc Medicine Aligns With FDA On Path Forward For Bitopertin In EPP

(RTTNews) - Disc Medicine, Inc. (IRON) announced it has completed a Type A meeting with the U.S. FDA regarding the CRL for its NDA of bitopertin in erythropoietic protoporphyria (EPP). The company con...

1 day ago - Nasdaq

Alterity Therapeutics (ATHE) Gets FDA Nod for Phase 3 Program

Alterity Therapeutics (ATHE) Gets FDA Nod for Phase 3 Program

1 day ago - GuruFocus

Alterity Therapeutics (ATHE) Secures FDA Agreement for Phase 3 ATH434 Trial

Alterity Therapeutics (ATHE) Secures FDA Agreement for Phase 3 ATH434 Trial

1 day ago - GuruFocus

Joe Lonsdale on SpaceX: A critical company in the middle of the biggest industrial revolution ever

Joe Lonsdale, 8VC founding partner and Palantir co-founder, joins 'Squawk Box' to discuss the upcoming SpaceX IPO, Nasdaq rule changes, state of the AI IPO race, FDA overhaul, and more.

1 day ago - CNBC

Watch CNBC's full interview with 8VC founding partner and Palantir co-founder Joe Lonsdale

Joe Lonsdale, 8VC founding partner and Palantir co-founder, joins 'Squawk Box' to discuss the upcoming SpaceX IPO, Nasdaq rule changes, state of the AI IPO race, FDA overhaul, and more.

1 day ago - CNBC

RedHill: FDA Grants Rare Pediatric Disease Designation To Opaganib

(RTTNews) - RedHill Biopharma Ltd. (RDHL) announced the FDA has granted rare pediatric disease designation to opaganib for treatment of neuroblastoma. The rare pediatric disease designation to opagani...

1 day ago - Nasdaq

Patanjali Foods receives notice from Maharashtra FDA over karela jamun juice claims

Patanjali Foods Limited has received a notice from the Joint Commissioner (Drugs), Food & Drug Administration, Maharashtra State, Nagpur Division, concerning promotional claims related to its Patanjal...

1 day ago - Business Upturn

Top Biotech Gainers: TNGX Hits New High, ALVO Moves Closer To FDA Approval, ZVRA, IDYA Turn Heads

(RTTNews) - Today's top gainers include Tango Therapeutics, following encouraging pancreatic cancer trial data; Aspire Biopharma, ahead of upcoming milestones; Alvotech, after FDA acceptance of its in...

1 day ago - Nasdaq

Medtronic Receives FDA Clearance for Nellcor Pulse Oximetry System With Nell-EQ Intelligent Processor, a New Technology Designed To Improve Reliability Across Diverse Patients and Conditions

This regulatory milestone follows news from earlier this year, when the company announced positive verification study results for its Nellcor pulse oximetry system with Nell-EQ intelligent processo...

2 days ago - Finanz Nachrichten

Pfizer: FDA Expands HYMPAVZI Approval To Pediatric And Inhibitor Hemophilia Patients

(RTTNews) - Pfizer Inc. (PFE) announced that the U.S. FDA has approved HYMPAVZI for additional patient groups: individuals aged 12 and older with hemophilia A or B who develop inhibitors, and children...

2 days ago - Nasdaq

Pfizer Says FDA Approves Expanded HYMPAVZI Indication For Hemophilia A And B

(RTTNews) - Pfizer, Inc. (PFE) announced Monday that the U.S. Food and Drug Administration (FDA) has approved an expanded indication for HYMPAVZI (marstacimab-hncq) to include the treatment of patient...

2 days ago - Nasdaq

Alvotech (ALVO) Secures FDA Review for New Biosimilar AVT16

Alvotech (ALVO) Secures FDA Review for New Biosimilar AVT16

2 days ago - GuruFocus