Medical Device Manufacturer · US , Cupertino , CA

Relign Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2017

Total

Cleared

Denied

Relign Corporation has 2 FDA 510(k) cleared medical devices. Based in Cupertino, US.

Last cleared in 2023. Active since 2017. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Relign Corporation

2 devices

1-2 of 2