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

Italy flag Italy · Delayed Price · Currency is EUR
0.2899
+0.0011 (0.38%)
Aug 13, 2025, 11:43 AM CET
0.38%
Market Cap2.16M
Revenue (ttm)17.53M
Net Income (ttm)-9.30M
Shares Out7.47M
EPS (ttm)-32.85
PE Ration/a
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volume36,431
Average Volume454,611
Open0.2820
Previous Close0.2888
Day's Range0.2810 - 0.2940
52-Week Range0.2000 - 26.4000
Beta0.05
RSI33.22
Earnings DateSep 11, 2025

About United States Steel

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

More than 20 GOP attorneys general call on RFK Jr, FDA to reinstate safeguards for abortion drugs

More than 20 Republican attorneys general are demanding that the Trump administration reinstate safety protocols for the abortion drug mifepristone.

2 hours ago - Fox News

FDA Grants 510(k) Clearance for Sonic Incytes’ Velacur ONE™, AI-Guided Point of Care Ultrasound for the Management of Chronic Liver Diseases

VANCOUVER, British Columbia — Sonic Incytes Medical Corp, proudly announces that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for Velacur ONE™, its point-of-care ultrasound...

14 hours ago - Financial Post

FDA may pull authorization of Pfizers Covid vaccine for children under 5

The potential move to rescind authorization of Pfizer's vaccine could leave some kids in the U.S. with no available shots against Covid.

15 hours ago - CNBC

Why Is Liquidia Stock Trading Higher On Tuesday?

Liquidia Corporation (NASDAQ: LQDA) reported on Tuesday a second-quarter loss of 49 cents, missing the consensus of a loss of 43 cents . See the LGDA stock price story here. Sales reached $8.84 milli...

16 hours ago - Benzinga

FDA Approves Insmed's Drug As First Treatment For Type Of Chronic Lung Disease

The FDA approves Insmed's Brinsupri for NCFB, ... Full story available on Benzinga.com

16 hours ago - Benzinga

CDC Shooting Linked To Suspect's COVID-19 Vaccine Beliefs, Former Staff Blame RFK Jr. Hostility Toward Agency

A group of former U.S. Centers for Disease Control and Prevention (CDC) employees are blaming HHS Secretary Robert F. Kennedy Jr. for vilifying the agency’s workforce through “his continuous lies abou...

16 hours ago - Benzinga

Top 5% Biotech, Insmed, Hits A Record High On Its 'Skeleton Key' Approval

Insmed stock hit a record high Tuesday after the FDA approved its drug, brensocatib, for patients with a devastating lung condition.

17 hours ago - Investor's Business Daily

Insmed wins FDA approval for lung disorder therapy Brinsupri

Insmed (INSM) stock rises as the FDA greenlights its lung disorder drug Brinsupri for patients with on-cystic fibrosis bronchiectasis. Read more here.

18 hours ago - Seeking Alpha

FDA Approves BRINSUPRI™ (brensocatib) as the First and Only Treatment for Non-Cystic Fibrosis Bronchiectasis, a Serious, Chronic Lung Disease

— Approximately 500,000 U.S. Patients Are Diagnosed with Non-Cystic Fibrosis Bronchiectasis (NCFB), a Progressive Disease That Can Lead to Permanent Lung Damage — — BRINSUPRI 10 mg and 25 mg Doses App...

19 hours ago - Benzinga

Altimmune Q2 FY2025 Earnings Call Transcript

Altimmune, Inc. (NASDAQ: ALT) reported its second-quarter financial results before Tuesday’s opening bell. Below are the transcripts from the Q2 earnings call. This transcript is brought to you by Be...

20 hours ago - Benzinga

Novartis Sees Hope In Reducing Lifelong Treatment Burden For Autoimmune Blood Disorder

Novartis AG (NYSE: NVS) released topline results on Tuesday from the VAYHIT2 Phase 3 trial evaluating ianalumab plus eltrombopag in patients with primary immune thrombocytopenia (ITP) previously trea...

20 hours ago - Benzinga

CalciMedica Reports Second Quarter 2025 Financial Results and Provides Clinical & Corporate Updates

Enrollment ongoing in Phase 2 KOURAGE trial of Auxora™ in acute kidney injury (AKI) with respiratory failure; data expected in early 2026 Productive initial meeting with the FDA on Auxora in acute pan...

23 hours ago - Benzinga

FDA May Not Renew Pfizer's Authorization For Covid Shots In Younger Children, Moderna Prepares To Boost Supply

View Preview Pfizer Inc.'s (NYSE: PFE) COVID-19 vaccine for children under five may lose U.S. Food and Drug Administration authorization this fall, raising the possibility of supply shortages and pro...

1 day ago - Benzinga

IO Biotech's Combo Therapy For Skin Cancer Falls Just Short, Eyes FDA Talks Later This Year

IO Biotech's Phase 3 trial showed ... Full story available on Benzinga.com

1 day ago - Benzinga

Vinay Prasad's Comeback To FDA Sparks Debate Over Regulatory Direction

In a stunning reversal, Dr. Vinay Prasad is returning to his role as director of the U.S. Food and Drug Administration’s (FDA) Center for Biologics Evaluation and Research (CBER), just days after his ...

1 day ago - Benzinga

FDA's vaccine chief returning to job a week after leaving: Report

CNBC's Joe Kernen reports on the latest news.

1 day ago - CNBC