Data / Medical devices / United Kingdom / Biopharm Uk Ltd
Biopharm Uk Ltd: FDA-registered device maker in HENDY Carmarthenshire, United Kingdom, 1 510(k) clearance
Biopharm Uk Ltd is registered with the FDA (registration 3008127439) in HENDY Carmarthenshire, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 19, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008127439
- Address
- 2 Bryngwili Road, HENDY Carmarthenshire, United Kingdom, SA4 0XT
- Owner or operator
- BIOPHARM UK LTD (10046286)
- Roles
- Manufacturer
- First device listed
- February 28, 2014
- Registered through
- 2026
- Brand names listed
- European Medical Leeches, European Medicinal Leeches, Medical Leeches, Medicinal Leeches
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Leeches, Medicinal | NRN | U | 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 |
|---|---|---|---|---|---|---|
| February 19, 2014 | K132958 | MEDICINAL LEECHES | NRN | Substantially Equivalent | Biopharm (Uk) , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated February 19, 2014. 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.