Microsurge, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microsurge, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Microsurge, Inc. has 15 FDA 510(k) cleared general & plastic surgery devices. Based in North Attleboro, US.
Historical record: 15 cleared submissions from 1991 to 1996.
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 - Microsurge, Inc.
15 devices
Cleared
Nov 27, 1996
MICROSURGE LAPAROSCOPIC PERMACLIP CARTRIDGE WITH IMPLANTABLE CLIP
General & Plastic Surgery
43d
Cleared
Mar 05, 1996
DETACHATIP THORACOSCOPIC SCISSORS
General & Plastic Surgery
25d
Cleared
Jan 31, 1996
MICROSURGE THORACOSCOPIC INSTRUMENTS
General & Plastic Surgery
65d
Cleared
Dec 28, 1995
ENDO-LEADER
General & Plastic Surgery
79d
Cleared
Oct 26, 1995
MICROSURGE PUNCTURE CLOSE DEVICE
General & Plastic Surgery
57d
Cleared
Oct 16, 1995
MICROSURGE VERESS NEEDLE
Obstetrics & Gynecology
18d
Cleared
Sep 29, 1995
MICROSURGE THORACOSCOPIC ACCESS SYSTEM
General & Plastic Surgery
86d
Cleared
Jun 14, 1995
MICROSURGE BIPOLAR GRASPERS
General & Plastic Surgery
86d
Cleared
Jun 10, 1994
MICROSURGE REUSABLE FRONT END GRASP DEVICES, MODIF
General & Plastic Surgery
330d
Cleared
Jun 08, 1993
MICROSURGE SUCTION/IRRIGATION SYSTEM CANNULAS
General & Plastic Surgery
134d
Cleared
May 17, 1993
MICROSURGE SUCTION/IRRIGATION SYSTEM
General & Plastic Surgery
181d
Cleared
Apr 07, 1993
MICROSURGE DETACHA-TIP SURGICAL INSTRUMENTS
General & Plastic Surgery
225d