Medical Device Manufacturer · US , Pittsburgh , PA

Kinetic Technology, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1988

Total

Cleared

Denied

Kinetic Technology, Inc. has 5 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.

Historical record: 5 cleared submissions from 1988 to 1992. Primary specialty: Physical Medicine.

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

Kinetic Technology, Inc. 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 - Kinetic Technology, Inc.

5 devices

1-5 of 5