Kingston Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kingston Technologies, Inc. - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
Kingston Technologies, Inc. has 5 FDA 510(k) cleared medical devices. Based in Dayton, US.
Historical record: 5 cleared submissions from 1988 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kingston Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kingston Technologies, Inc.
6 devices
Cleared
Jul 20, 1994
HYDROTORQUE GUIDE WIRE
Cardiovascular
261d
Cleared
May 12, 1994
HYDRO-M(TM) WOUND GEL
General & Plastic Surgery
79d
Cleared
May 06, 1994
KTI HY-Q(TM) WOUND DRESSING
General & Plastic Surgery
78d
Cleared
Apr 20, 1993
KTI TRANSPARENT WOUND DRESSING
General & Plastic Surgery
161d
Cleared
Sep 29, 1992
HYSORB WOUND DRESSING
General & Plastic Surgery
182d
Cleared
Aug 02, 1988
PANAMEX(TM) URETERAL STENT
Gastroenterology & Urology
71d