Medical Device Manufacturer · FR , Chaville

Sas Oniris - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2016

Total

Cleared

Denied

Sas Oniris has 1 FDA 510(k) cleared medical devices. Based in Chaville, FR.

Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Dental.

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

Sas Oniris is one of 153 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sas Oniris

1 devices

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