Medical Device Manufacturer · US , Walker , MI

Markoptic - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1983
2
Total
2
Cleared
0
Denied

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

Historical record: 2 cleared submissions from 1983 to 1986. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Markoptic
2 devices
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