Kinsa, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kinsa, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Kinsa QuickCare Thermometer
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Kinsa, Inc.
2 devices