Data / Medical devices / United Kingdom / Oxford Brain Diagnostics, Ltd.
Oxford Brain Diagnostics, Ltd.: FDA-registered device maker in Oxford, United Kingdom, 1 510(k) clearance
Oxford Brain Diagnostics, Ltd. is registered with the FDA (registration 3035386366) in Oxford, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 6, 2024. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3035386366
- Address
- Blue Boar Court 9 Alfred Street, Oxford, United Kingdom, OX1 4EH
- Owner or operator
- Oxford Brain Diagnostics, Ltd. (10092378)
- Roles
- Manufacturer
- First device listed
- December 30, 2024
- Registered through
- 2026
- Brand names listed
- CDM Insights
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Automated Radiological Image Processing Software | QIH | 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 6, 2024 | K240680 | CDM Insights | QIH | Substantially Equivalent | Oxford Brain Diagnostics, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated December 6, 2024. 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.