Gyne-Tech Instrument Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gyne-Tech Instrument Corp. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Gyne-Tech Instrument Corp. has 3 FDA 510(k) cleared medical devices. Based in Burbank, US.
Historical record: 3 cleared submissions from 1992 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Gyne-Tech Instrument Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gyne-Tech Instrument Corp.
3 devices