Medical Device Manufacturer · US , Creve Coeur , MO

Biomechanic, Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 1995

Total

Cleared

Denied

Biomechanic, Inc. has 0 FDA 510(k) cleared medical devices. Based in Creve Coeur, US.

Historical record: 0 cleared submissions from 1995 to 1995. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Biomechanic, Inc.

1 devices

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