Medical Device Manufacturer · US , Port Ludlow , WA

Opti-Max - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1995

Total

Cleared

Denied

Opti-Max has 6 FDA 510(k) cleared medical devices. Based in Port Ludlow, US.

Historical record: 6 cleared submissions from 1995 to 1997. Primary specialty: Dental.

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

Opti-Max is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Opti-Max

6 devices

1-6 of 6