Medical Device Manufacturer · US , Menlo Park , CA

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

3 submissions · 3 cleared · Since 2014

Total

Cleared

Denied

Spirox, Inc. has 3 FDA 510(k) cleared medical devices. Based in Menlo Park, US.

Historical record: 3 cleared submissions from 2014 to 2016. Primary specialty: Ear, Nose, Throat.

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

Spirox, Inc. is one of 4782 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

3 devices

1-3 of 3