Medical Device Manufacturer · US , New York , NY

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

2 submissions · 2 cleared · Since 2013

Total

Cleared

Denied

Kinsa, Inc. has 2 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 2 cleared submissions from 2013 to 2018. Primary specialty: General Hospital.

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

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

2 devices

1-2 of 2