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

Italy flag Italy · Delayed Price · Currency is EUR
0.1266
-0.0034 (-2.62%)
Dec 12, 2025, 5:29 PM CET
-98.09%
Market Cap1.89M
Revenue (ttm)21.13M
Net Income (ttm)-2.19M
Shares Out14.90M
EPS (ttm)-1.15
PE Ration/a
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volume897,977
Average Volume1,590,174
Open0.1269
Previous Close0.1300
Day's Range0.1207 - 0.1299
52-Week Range0.1075 - 7.3000
Beta-0.03
RSI32.10
Earnings DateNov 14, 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]

Founded 1974
Employees 159
Stock Exchange Borsa Italiana
Ticker Symbol FDA
Full Company Profile

Financial Performance

In 2024, Fidia's revenue was 17.53 million, a decrease of -38.98% compared to the previous year's 28.74 million. Losses were -9.30 million, 611.4% more than in 2023.

Financial Statements

News

FDA Approves Innoviva's NUZOLVENCE, First-in-Class Oral Treatment For Gonorrhea

(RTTNews) - Innoviva Specialty Therapeutics, a subsidiary of Innoviva, Inc. (INVA), announced that the U.S. Food and Drug Administration approved NUZOLVENCE (zoliflodacin) for oral suspension, a first...

5 hours ago - Nasdaq

FDA Approves Milestone Pharma' CARDAMYST, First Self-Administered Treatment For PSVT

(RTTNews) - Milestone Pharmaceuticals Inc. (MIST) announced that the U.S. Food and Drug Administration has approved its first commercial product, CARDAMYST (etripamil) nasal spray. The prescription me...

5 hours ago - Nasdaq

FDA Approves Johnson & Johnson's AKEEGA For BRCA2-Mutated Prostate Cancer

(RTTNews) - Johnson & Johnson (JNJ) announced that the U.S. Food and Drug Administration has approved its supplemental New Drug Application (sNDA) for AKEEGA—a dual-action tablet combining niraparib a...

7 hours ago - Nasdaq

INVA: FDA Approves Innoviva's Nuzolvence for Gonorrhea Treatment

INVA: FDA Approves Innoviva's Nuzolvence for Gonorrhea Treatment

10 hours ago - GuruFocus

ABBV Stock News: Lenz Therapeutics Faces Setback with FDA Report

ABBV Stock News: Lenz Therapeutics Faces Setback with FDA Report

12 hours ago - GuruFocus

FDA Grants Orphan Status to Amgen's (AMGN) Blinatumomab for Leukemia Treatment

FDA Grants Orphan Status to Amgen's (AMGN) Blinatumomab for Leukemia Treatment

12 hours ago - GuruFocus

FDA Expands Use of Johnson & Johnson's Akeega for Prostate Cancer

FDA Expands Use of Johnson & Johnson's Akeega for Prostate Cancer

13 hours ago - GuruFocus

FDA Approval Boosts Johnson & Johnson's (JNJ) Prostate Cancer Treatment

FDA Approval Boosts Johnson & Johnson's (JNJ) Prostate Cancer Treatment

13 hours ago - GuruFocus

Maharashtra Needs 771 FDA Officials As Per Union Norms, 42 Posts Filled: FDA Minister

Nagpur: Amid concerns over Pakistan-manufactured cosmetic products infiltrating Indian markets, the Maharashtra Food and Drug Administration (FDA) is .

13 hours ago - The Times of India

Healthy Returns: FDA may add its strongest safety warning to Covid vaccines. Here’s what to know

The FDA is reportedly preparing to add what's known as a "black box" warning to Covid shots by the end of the year, marking a major shift in vaccine oversight.

14 hours ago - CNBC

European Regulator Backs Approval Of Novo Nordisk High-Dose Wegovy

On Friday, the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) issued a positive opinion for Novo Nordisk A/S’ (NYSE: NVO) higher dose of Wegovy (semaglutide 7...

14 hours ago - Benzinga

FDA Weighs Black Box Warning For COVID Vaccines, Experts Push Back

The U.S. Food and Drug Administration (FDA) is reportedly considering adding a boxed warning — the agency's highest-level safety alert — to Covid-19 vaccines , a move that has drawn immediate criticis...

14 hours ago - Benzinga

Fake medicine scare: 11 hosps flagged, 538 shops inspected, reveals FDA min

Nagpur: The state's Food and Drug Administration minister Narhari Zirwal on Friday confirmed major irregularities in the procurement and circulation o.

14 hours ago - The Times of India

ImmunityBio Moves Closer To EU Approval For Bladder Cancer Therapy

The European Medicines Agency has recommended granting a conditional marketing authorization for ImmunityBio, Inc. ‘s (NASDAQ: IBRX) Anktiva (nogapendekin alfa inbakicept) in combination with Bacillu...

15 hours ago - Benzinga

Can Opdivo's Label Expansions Help Bristol Myers Sustain Its Momentum?

BMY gets a priority FDA review for Opdivo's use in previously untreated advanced Hodgkin lymphoma, reinforcing its oncology momentum.

17 hours ago - Nasdaq

Kymera's Eczema Drug Gets Fast Track Designation in the United States

KYMR gains momentum as the FDA grants Fast Track to KT-621 for moderate to severe atopic dermatitis, boosting the stock and advancing its Type 2 pipeline.

17 hours ago - Nasdaq

BioCryst Gets FDA Approval To Treat Rare Childhood Swelling Disorder With Oral Drug

The U.S. Food and Drug Administration (FDA) on Friday approved BioCryst Pharmaceuticals Inc.’s (NASDAQ: BCRX) New Drug Application (NDA) for the use of an oral pellet formulation of once-daily Orlade...

17 hours ago - Benzinga

FDA Approves Acadia's DAYBUE STIX Powder For Oral Solution For Rett Syndrome

(RTTNews) - Acadia Pharmaceuticals Inc. (ACAD) announced that the FDA has approved DAYBUE STIX for oral solution for the treatment of Rett syndrome in adult and pediatric patients two years of age and...

17 hours ago - Nasdaq

GSK Gets FDA Nod for Blujepa in Uncomplicated Urogenital Gonorrhea

GSK wins FDA approval for Blujepa, a new oral antibiotic treatment option for uncomplicated urogenital gonorrhea.

17 hours ago - Nasdaq

CBLL Gets FDA Consent for One-of-a-Kind Delirium Monitoring Solution

CeriBell gains FDA clearance for its continuous delirium monitoring solution, boosting its AI-driven EEG platform and expanding its role in critical care.

17 hours ago - Nasdaq

Amgen (AMGN) Gains FDA Nod for Expanded Use of Uplizna in Myasthenia Gravis

Amgen (AMGN) Gains FDA Nod for Expanded Use of Uplizna in Myasthenia Gravis

18 hours ago - GuruFocus

FDA Weighs Rapid Review For Eli Lilly Obesity Pill As Novo Nordisk Nears Launch

FDA may expedite approval timeline for ... Full story available on Benzinga.com

19 hours ago - Benzinga

BioCryst's Orladeyo Oral Pellets Win FDA Nod For HAE Patients 2 To Under 12

(RTTNews) - BioCryst Pharmaceuticals, Inc. (BCRX) announced that the FDA has approved Orladeyo oral pellets for prophylactic treatment of hereditary angioedema or HAE in pediatric patients aged 2 to u...

19 hours ago - Nasdaq

FDA Approves Acadia's Powder Formulation Of DAYBUE For Rett Syndrome

(RTTNews) - Acadia Pharmaceuticals Inc. (ACAD) on Friday announced that the U.S. Food and Drug Administration (FDA) has approved DAYBUE STIX, a powder formulation of DAYBUE oral solution, for the trea...

19 hours ago - Nasdaq

FDA Approves New Formulation for Acadia Pharmaceuticals' (ACAD) Rett Syndrome Treatment

FDA Approves New Formulation for Acadia Pharmaceuticals' (ACAD) Rett Syndrome Treatment

19 hours ago - GuruFocus