Data / Medical devices / Turkey / Bimed Teknik Aletler Sanayi & Ticaret A.S.
Bimed Teknik Aletler Sanayi & Ticaret A.S.: FDA-registered device maker in Beylikduzu Istanbul, Turkey, 1 510(k) clearance
Bimed Teknik Aletler Sanayi & Ticaret A.S. is registered with the FDA (registration 3009551627) in Beylikduzu Istanbul, Turkey. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 3, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3009551627
- Address
- BeylikduzuOSB Mahallesi Leylak Caddesi No:16, Beylikduzu Istanbul, Turkey, 34520
- Owner or operator
- BIMED TEKNIK (10049215)
- Roles
- Manufacturer
- First device listed
- August 5, 2025
- Registered through
- 2027
- Brand names listed
- 3DOSE 1ml Syringe
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Syringe, Piston | FMF | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 3, 2025 | K250733 | 3DOSE 1ml Syringe | FMF | Substantially Equivalent | Bimed Teknik Aletler Sanayi & Ticaret A.S. | accessdata.fda.gov |
Compare with other makers
Updated July 3, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.