Medical Device Manufacturer · US , Irvine , CA

Dioptics - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1986

Total

Cleared

Denied

Dioptics has 6 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 6 cleared submissions from 1986 to 1990. Primary specialty: Ophthalmic.

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

Dioptics 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 - Dioptics

6 devices

1-6 of 6