Medical Device Manufacturer · US , Minnetonka , MN

Flex Medics Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1993
1
Total
1
Cleared
0
Denied

Flex Medics Corporation has 1 FDA 510(k) cleared medical devices. Based in Minnetonka, US.

Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Flex Medics Corporation

1 devices
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