Medical Device Manufacturer · US , Redmond , WA

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

5 submissions · 5 cleared · Since 2015

Total

Cleared

Denied

Spiration, Inc. has 5 FDA 510(k) cleared medical devices. Based in Redmond, US.

Historical record: 5 cleared submissions from 2015 to 2017. Primary specialty: Ear, Nose, Throat.

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

Spiration, Inc. is one of 15061 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5