Medical Device Manufacturer · US , Edison , NJ

Technidyne Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1993

Total

Cleared

Denied

Technidyne Corp. has 2 FDA 510(k) cleared medical devices. Based in Edison, US.

Historical record: 2 cleared submissions from 1993 to 1993. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Technidyne Corp. Filter by specialty or product code using the sidebar.

Technidyne Corp. 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 - Technidyne Corp.

2 devices

1-2 of 2