Medical Device Manufacturer · CA , Canada

Oculo-Plastik Reg'D - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1987

Total

Cleared

Denied

Oculo-Plastik Reg'D has 1 FDA 510(k) cleared medical devices. Based in Canada, CA.

Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Oculo-Plastik Reg'D Filter by specialty or product code using the sidebar.

Oculo-Plastik Reg'D is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Oculo-Plastik Reg'D

1 devices

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