Ndo Surgical, Inc. is one of 15070 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ndo Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PLICATOR GSX SUTURING SYSTEM, PLICATOR GSX, PLICATOR INSTRUMENT, PLICATOR GSX SUTURE CARTRIDGE, ENDOSCOPIC PLICATION SYSTEM, EPS, EPLICATOR, PLICATOR INSTRUMENT, ENDOSCOPIC PLICATION SYSTEM
6
Total
6
Cleared
0
Denied
Ndo Surgical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mansfield, US.
Historical record: 6 cleared submissions from 2003 to 2008. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Ndo Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ndo Surgical, Inc.
6 devices
Cleared
Mar 26, 2008
PLICATOR GSX SUTURING SYSTEM, PLICATOR GSX, PLICATOR INSTRUMENT, PLICATOR GSX...
Gastroenterology & Urology
90d
Cleared
Oct 18, 2007
ENDOSCOPIC PLICATION SYSTEM, EPS, EPLICATOR, PLICATOR INSTRUMENT
Gastroenterology & Urology
77d
Cleared
Sep 18, 2007
ENDOSCOPIC PLICATION SYSTEM
Gastroenterology & Urology
104d
Cleared
Oct 23, 2003
MODIFICATION TO ENDOSCOPIC PLICATION SYSTEM
Gastroenterology & Urology
43d
Cleared
May 23, 2003
ENDOSCOPIC PLICATION SYSTEM, MODEL 160-00760
Gastroenterology & Urology
32d
Cleared
Apr 17, 2003
ENDOSCOPIC PLICATION SYSTEM
General & Plastic Surgery
202d