Medical Device Manufacturer · CA , Canada L4v 1p1

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

2 submissions · 2 cleared · Since 1987

Total

Cleared

Denied

Allelix, Inc. has 2 FDA 510(k) cleared medical devices. Based in Canada L4v 1p1, CA.

Historical record: 2 cleared submissions from 1987 to 1987. Primary specialty: Microbiology.

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

Allelix, 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 - Allelix, Inc.

2 devices

1-2 of 2