Medical Device Manufacturer · GB , England

Kenex , Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1995

Total

Cleared

Denied

Kenex , Ltd. has 4 FDA 510(k) cleared medical devices. Based in England, GB.

Historical record: 4 cleared submissions from 1995 to 1995. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Kenex , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kenex , Ltd.

4 devices

1-4 of 4