Medical Device Manufacturer · US , Camarillo , CA

Kinamed, Incorporated - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011

Total

Cleared

Denied

Kinamed, Incorporated has 2 FDA 510(k) cleared medical devices. Based in Camarillo, US.

Historical record: 2 cleared submissions from 2011 to 2018. Primary specialty: Orthopedic.

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

Kinamed, Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kinamed, Incorporated

2 devices

1-2 of 2