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

FDA 510(k) Regulatory Record - Dyonics, Inc. Neurology ✕

3 devices

1-3 of 3

Cleared Nov 17, 1988

DYNAMIC CRUCIATE TESTER

Neurology · 197d

Cleared Feb 20, 1987

ARTHROSCOPIC SHOULDER HOLDER

Neurology · 31d

Cleared Apr 05, 1979

DYONICS STEROTOXIC POSITIONER

Neurology · 23d