Data / Medical devices / United Kingdom / Biometrics Ltd.
Biometrics Ltd.: FDA-registered device maker in Newport Wales, United Kingdom, 2 510(k) clearances
Biometrics Ltd. is registered with the FDA (registration 8021957) in Newport Wales, United Kingdom. It lists 7 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 11, 1996. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8021957
- FEI number
- 3768
- Address
- Nine Mile Point Ind. Estate Units 25-26, Newport Wales, United Kingdom, NP11 7HZ
- Owner or operator
- BIOMETRICS LTD (8021957)
- Roles
- Manufacturer
- First device listed
- October 19, 1992
- Registered through
- 2026
- Brand names listed
- A1000, A1500, A500, AC1500M, AC1500S, ACL500 Wireless accelerometer, AD1 Wireless Adaptor, AD2 Wireless Adapter and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cable | ISN | 1 | Manufacturer | accessdata.fda.gov |
| Device, Biofeedback | HCC | 2 | Manufacturer | accessdata.fda.gov |
| Exerciser, Measuring | ISD | 2 | Manufacturer | accessdata.fda.gov |
| Exerciser, Non-Measuring | ION | 1 | Manufacturer | accessdata.fda.gov |
| Exerciser, Powered | BXB | 1 | Manufacturer | accessdata.fda.gov |
| Goniometer, Ac-Powered | KQX | 1 | Manufacturer | accessdata.fda.gov |
| System, Isokinetic Testing And Evaluation | IKK | 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 |
|---|---|---|---|---|---|---|
| December 11, 1996 | K962855 | ULE-2, MULE-2, HAND ACCESSORY KIT | ISD | Substantially Equivalent | Penny and Giles Biometrics , Ltd. | accessdata.fda.gov |
| December 19, 1988 | K884003 | GONIOMETER AND BIOMEDICAL RECORDER SYSTEM | KQX | Substantially Equivalent | Penny & Giles Blackwood , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Exerciser, Measuring
- All makers of Cable
- All makers of System, Isokinetic Testing And Evaluation
- All makers of Exerciser, Powered
- All makers of Exerciser, Non-Measuring
- All makers of Device, Biofeedback
Updated December 11, 1996. 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.