Medical Device Manufacturer · US , Irvine , CA

Allez Spine, LLC - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2005

Total

Cleared

Denied

Allez Spine, LLC has 7 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 7 cleared submissions from 2005 to 2009. Primary specialty: Orthopedic.

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

Allez Spine, LLC is one of 20736 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Allez Spine, LLC

7 devices

1-7 of 7