Medical Device Manufacturer · US , Brewster , NY

Dynarex Corp. - FDA 510(k) Cleared Devices

19 submissions · 18 cleared · Since 1986
19
Total
18
Cleared
0
Denied

Dynarex Corp. has 18 FDA 510(k) cleared medical devices. Based in Brewster, US.

Historical record: 18 cleared submissions from 1986 to 2005. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) Regulatory Record - Dynarex Corp.
19 devices
1-12 of 19
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