Medical Device Manufacturer · US , Long Grove , IL

Oculon Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1992

Total

Cleared

Denied

Oculon Corp. has 1 FDA 510(k) cleared medical devices. Based in Long Grove, US.

Historical record: 1 cleared submissions from 1992 to 1992. Primary specialty: Ophthalmic.

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

Oculon Corp. 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 - Oculon Corp.

1 devices

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