Data / Medical devices / United Kingdom / Bering Limited
Bering Limited: FDA-registered device maker in London London, City of, United Kingdom, 1 510(k) clearance
Bering Limited is registered with the FDA (registration 3034205378) in London London, City of, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 9, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3034205378
- Address
- 54 Portland Plance, London London, City of, United Kingdom, W1B1DY
- Owner or operator
- Bering Limited (10092078)
- Roles
- Manufacturer
- First device listed
- December 2, 2024
- Registered through
- 2026
- Brand names listed
- BraveCX
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Radiological Computer-Assisted Prioritization Software For Lesions | QFM | 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 |
|---|---|---|---|---|---|---|
| November 9, 2023 | K223754 | BraveCX | QFM | Substantially Equivalent | Bering, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated November 9, 2023. 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.