Medical Device Manufacturer · US , Los Angeles , CA

Eyeworks 3 - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1993

Total

Cleared

Denied

Eyeworks 3 has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Historical record: 2 cleared submissions from 1993 to 1993. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Eyeworks 3 Filter by specialty or product code using the sidebar.

Eyeworks 3 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 - Eyeworks 3

2 devices

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