Aslan Medical Technologies, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aslan Medical Technologies, Ltd. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Aslan Medical Technologies, Ltd. has 8 FDA 510(k) cleared medical devices. Based in Oakland, US.
Historical record: 8 cleared submissions from 1992 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aslan Medical Technologies, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aslan Medical Technologies, Ltd.
8 devices
Cleared
Aug 06, 1998
ASLAN SENSOR MODULAR INSTRUMENT
General & Plastic Surgery
37d
Cleared
Feb 09, 1996
ASLAN MODULAR INSTRUMENT
General & Plastic Surgery
109d
Cleared
Jun 12, 1995
ASLAN LAPRETRACT
General & Plastic Surgery
28d
Cleared
Mar 14, 1995
ASLAN KNOT PUSHER
Gastroenterology & Urology
13d
Cleared
Sep 13, 1994
ASLAN DUAL ACTION JAWS GRASPING FORCEPS
General & Plastic Surgery
22d
Cleared
Mar 09, 1993
MCKERNAN-ADSON AGGRESSIVE FORCEPS
General & Plastic Surgery
85d
Cleared
Mar 09, 1993
MCKERNAN-POTTS GRASPING FORCEPS
General & Plastic Surgery
85d
Cleared
Nov 25, 1992
MCKERNAN ATRAUMATIC FORCEPS
General & Plastic Surgery
51d