Medical Device Manufacturer · US , Round Rock , TX

Teknimed, S.A. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2003

Total

Cleared

Denied

Teknimed, S.A. has 11 FDA 510(k) cleared orthopedic devices. Based in Round Rock, US.

Historical record: 11 cleared submissions from 2003 to 2011.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Teknimed, S.A.

11 devices

1-11 of 11

OPACITY + BONE CEMENT

SPINE-FIX BIOMIMETIC BONE CEMENT

CERAFORM BONE VOID FILLER

CEMSTOP CEMENT RESTRICTOR

K032685 · LZN

Orthopedic · 89d

Teknimed, S.A. - FDA 510(k) Cleared Devices

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