Medical Device Manufacturer · US , Walker , MI

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

19 submissions · 19 cleared · Since 1978
19
Total
19
Cleared
0
Denied

Dyonics, Inc. has 19 FDA 510(k) cleared orthopedic devices. Based in Walker, US.

Historical record: 19 cleared submissions from 1978 to 1990.

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 - Dyonics, Inc.
19 devices
1-12 of 19
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