Medical Device Manufacturer · US , Palo Alto , CA

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

1 submissions · 1 cleared · Since 2016

Total

Cleared

Denied

Syntorr, Inc. has 1 FDA 510(k) cleared medical devices. Based in Palo Alto, US.

Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Syntorr, Inc.

1 devices

1-1 of 1