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

Italy flag Italy · Delayed Price · Currency is EUR
0.0529
-0.0021 (-3.82%)
At close: Mar 6, 2026
-94.91%
Market Cap 819.50K
Revenue (ttm) 21.13M
Net Income (ttm) -2.19M
Shares Out 14.90M
EPS (ttm) -1.15
PE Ratio n/a
Forward PE n/a
Dividend n/a
Ex-Dividend Date n/a
Volume 2,729,453
Average Volume 1,476,442
Open 0.0559
Previous Close 0.0550
Day's Range 0.0529 - 0.0568
52-Week Range 0.0500 - 1.0600
Beta 0.03
RSI 11.46
Earnings Date Mar 13, 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]

Sector Industrials
Founded 1974
Employees 140
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

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FDA reversals leave investors worrying about the fates of other experimental drugs

Investors are scrutinizing the prospects for some drugs in the pipeline following a string of recent rejections from the U.S. Food and Drug Administration.

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Weekly Buzz: TBPH Cuts Jobs, ASND Gets FDA Nod, AARD Puts HERO On Hold, ESPR Opens Wallet

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Halozyme Says J&J Wins FDA Approval For Tecvayli, Darzalex Faspro Combo In Multiple Myeloma

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11 hours ago - Nasdaq

Immuneering Reports Fourth Quarter and Full Year 2025 Financial Results and Provides Business Updates

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12 hours ago - Benzinga

FDA Roundup: First-Line Hernexeos, Weekly Yuviwel, Expanded Palynziq & Sogroya Indications

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uniQure (QURE) Faces FDA Demand for Phase 3 Trial for Huntington's Drug

uniQure (QURE) Faces FDA Demand for Phase 3 Trial for Huntington's Drug

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Outlook Therapeutics (OTLK) Advances Towards FDA Approval for ONS-5010

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1 day ago - GuruFocus

Johnson & Johnson (JNJ) Gains FDA Approval for New Multiple Myeloma Treatment

Johnson & Johnson (JNJ) Gains FDA Approval for New Multiple Myeloma Treatment

1 day ago - GuruFocus

FDA Approves J&J's Tecvayli for Multiple Myeloma Treatment

FDA Approves J&J's Tecvayli for Multiple Myeloma Treatment

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FDA official calls UniQure's gene therapy a 'failed' treatment for Huntington's disease

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1 day ago - CNBC

uniQure's (QURE) Gene Therapy for Huntington's Disease Faces FDA Setback

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Johnson & Johnson (JNJ) Gets FDA Nod for Tec-Dara in Multiple Myeloma Treatment

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Trust in CDC, FDA, NIH shrinks: Survey

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1 day ago - The Hill

FDA Defends Call For Placebo Study In uniQure Huntington's Gene Therapy Trial

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1 day ago - Benzinga

‘Usually everybody loves money’: Trump’s FDA chief to start giving bonuses for faster drug reviews

The FDA lost about 20% of its workforce after Trump took office last year. Now it wants to shrink approvals from as long as 29 months to as low as six.

1 day ago - Fortune

UniQure (QURE) Faces FDA Hurdle for Huntington's Disease Therapy

UniQure (QURE) Faces FDA Hurdle for Huntington's Disease Therapy

1 day ago - GuruFocus

SeaStar Medical Completes FDA Enrollment Requirement For SAVE Registry In Pediatric AKI

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Next-Generation Cancer Therapies Post Breakthrough Results Across Multiple Tumor Types

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REGENXBIO Reports Fourth Quarter and Full Year 2025 Financial Results and Operational Highlights

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Lilly Employer Connect platform launches with over fifteen independent program administrators offering tailored obesity coverage options to expand access to patients

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Estrogen patches harder to find as FDA pushes hormone therapy

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1 day ago - The Hill

FDA Places Partial Hold On PepGen's Myotonic Dystrophy Drug Trial

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1 day ago - Benzinga

Granules India subsidiary receives US FDA EIR with NAI status for Virginia facility

Granules India Limited announced that its US step-down subsidiary, Granules Consumer Health, LLC, has received an Establishment Inspection Report (EIR) with a No Action Indicated (NAI) status from the...

1 day ago - Business Upturn