Medical Device Manufacturer · US , Redwood City , CA

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

3 submissions · 3 cleared · Since 2016

Total

Cleared

Denied

Arrinex, Inc. has 3 FDA 510(k) cleared medical devices. Based in Redwood City, US.

Historical record: 3 cleared submissions from 2016 to 2019. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Arrinex, Inc.

3 devices

1-3 of 3