Medical Device Manufacturer · US , Rockleigh , NJ

Optimaxx Intl. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997
1
Total
1
Cleared
0
Denied

Optimaxx Intl. has 1 FDA 510(k) cleared medical devices. Based in Rockleigh, US.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Ophthalmic.

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

FDA 510(k) Regulatory Record - Optimaxx Intl.

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