Medical Device Manufacturer · CA , Quebec

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

3 submissions · 3 cleared · Since 2000

Total

Cleared

Denied

Amylior, Inc. has 3 FDA 510(k) cleared medical devices. Based in Quebec, CA.

Historical record: 3 cleared submissions from 2000 to 2009. Primary specialty: Physical Medicine.

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

Amylior, 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 - Amylior, Inc.

3 devices

1-3 of 3