Data / Medical devices / United Kingdom / Owen Mumford Limited
Owen Mumford Limited: FDA-registered device maker in Witney Oxfordshire, United Kingdom, 1 510(k) clearance
Owen Mumford Limited is registered with the FDA (registration 3038110468) in Witney Oxfordshire, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 17, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3038110468
- Address
- De Havilland Way, Witney Oxfordshire, United Kingdom, OX29 0YG
- Owner or operator
- OWEN MUMFORD LTD. (8021764)
- Roles
- Manufacturer
- First device listed
- November 1, 2021
- Registered through
- 2026
- Brand names listed
- Unifine SafeControl, Unifine Ultra
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Hypodermic, Single Lumen | FMI | 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 |
|---|---|---|---|---|---|---|
| September 17, 2021 | K210399 | Unifine SafeControl | FMI | Substantially Equivalent | Owen Mumford, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 17, 2021. 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.