Data / Medical devices / United Kingdom / Minta Medical Limited
Minta Medical Limited: FDA-registered device maker in MERSEYSIDE Knowsley, United Kingdom, 1 510(k) clearance
Minta Medical Limited is registered with the FDA (registration 3004617090) in MERSEYSIDE Knowsley, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 14, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004617090
- Address
- Caddick Road, MERSEYSIDE Knowsley, United Kingdom, L34 9HP
- Owner or operator
- MINTA MEDICAL LIMITED (9064097)
- Roles
- Manufacturer
- First device listed
- November 23, 2012
- Registered through
- 2026
- Brand names listed
- ADAPTER CABLE, DISPOSABLE RF ELECTRODE, DISPOSABLE RF THERMOCOUPLE ELECTRODE, MINTA RYAN RF THERMOCOUPLE ELECTRODE, NITINOL RADIOFREQUENCY ELECTRODE, NITINOL RADIOFREQUENCY LESION PROBE, NITINOL RADIOFREQUENCY THERMOCOUPLE ELECTRODE, NITINOL REUSABLE RADIOFREQUENCY ELECTRODE and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Probe, Radiofrequency Lesion | GXI | 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 |
|---|---|---|---|---|---|---|
| June 14, 2010 | K090608 | MINTA RYAN RF THERMOCOUPLE ELECTRODE (RYAN-50, 100, 150 AND 200), MINTA INTERMEDIATE CABLE (RYAN-C, -R, -B) | GXI | Substantially Equivalent | Minta Medical Limited | accessdata.fda.gov |
Compare with other makers
Updated June 14, 2010. 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.