Endoscopic Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endoscopic Technologies, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Endoscopic Technologies, Inc. has 8 FDA 510(k) cleared medical devices. Based in Norcross, US.
Historical record: 8 cleared submissions from 1993 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Endoscopic Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Endoscopic Technologies, Inc.
8 devices
Cleared
May 10, 2006
ESTECH AORTIC EASY FLOW CANNULA
Cardiovascular
118d
Cleared
Jan 06, 2006
ESTECH COBRA ELECTROSURGICAL UNIT & CABLE
General & Plastic Surgery
36d
Cleared
Dec 19, 2005
ESTECH COBRA BIPOLAR SYSTEM
General & Plastic Surgery
46d
Cleared
Apr 06, 1995
ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES
General & Plastic Surgery
113d
Cleared
Jan 11, 1995
TUBING, NONINVASIVE
General Hospital
34d
Cleared
Dec 21, 1994
TROCAR/CANNULA
General & Plastic Surgery
13d
Cleared
Mar 11, 1994
DISPOSIBLE ELECTRO COAGULATION PROBE
General & Plastic Surgery
576d
Cleared
Apr 05, 1993
TROCARS
General & Plastic Surgery
305d