Medical Device Manufacturer · US , Walker , MI

Dynasplint Systems, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1982

Total

Cleared

Denied

Dynasplint Systems, Inc. has 2 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 2 cleared submissions from 1982 to 1991. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Dynasplint Systems, Inc.

2 devices

1-2 of 2