Unisurge, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Unisurge, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Unisurge, Inc. has 12 FDA 510(k) cleared general & plastic surgery devices. Based in Mountain View, US.
Historical record: 12 cleared submissions from 1992 to 1994.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Unisurge, Inc.
12 devices
Cleared
Oct 07, 1994
UNIGRIP
General & Plastic Surgery
93d
Cleared
Nov 12, 1993
INSTRUMENT ACTUATING DEVICE (IAD)
General & Plastic Surgery
102d
Cleared
Oct 08, 1993
APPLIER, SURGICAL, CLIP
General & Plastic Surgery
245d
Cleared
Aug 11, 1993
OBGRIP AND UNITIPS(TM)
General & Plastic Surgery
184d
Cleared
Aug 10, 1993
UNITIPS SURGICAL INSTRUMENTS
General & Plastic Surgery
264d
Cleared
Aug 10, 1993
UNICHANNEL(TM SURGICAL GRASPER
General & Plastic Surgery
260d
Cleared
Aug 10, 1993
UNITIPS
General & Plastic Surgery
175d
Cleared
Aug 10, 1993
UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC
General & Plastic Surgery
74d
Cleared
May 17, 1993
UNITROCAR(TM) REUSABLE SURG TROCAR/RESUSE KIT
General & Plastic Surgery
151d
Cleared
Apr 20, 1993
UNICLIP SURGICAL CLIP APPLIER
General & Plastic Surgery
132d
Cleared
Sep 21, 1992
UNISURGE DISPOSABLE TROCAR
Obstetrics & Gynecology
322d
Cleared
Apr 06, 1992
MANUAL SURGICAL INSTRMENTS FOR LAPAROSCOPY
General & Plastic Surgery
131d