Medical Device Manufacturer · US , Grand Junction , CO

Opti-Centre Laboratories - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1998

Total

Cleared

Denied

Opti-Centre Laboratories has 6 FDA 510(k) cleared medical devices. Based in Grand Junction, US.

Historical record: 6 cleared submissions from 1998 to 2005. Primary specialty: Ophthalmic.

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

Opti-Centre Laboratories 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-Centre Laboratories

6 devices

1-6 of 6