Medical Device Manufacturer · CA , Laval, Quebec

Orsonique, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1996

Total

Cleared

Denied

Orsonique, Inc. has 6 FDA 510(k) cleared medical devices. Based in Laval, Quebec, CA.

Historical record: 6 cleared submissions from 1996 to 1997. Primary specialty: Ear, Nose, Throat.

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

Orsonique, Inc. 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 - Orsonique, Inc.

6 devices

1-6 of 6