Aragon Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aragon Surgical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Aragon Surgical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Historical record: 6 cleared submissions from 2007 to 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aragon Surgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aragon Surgical, Inc.
6 devices
Cleared
Jul 11, 2011
ARAGON SURGICAL RF SYSTEM - 5MM LAPAROSCOPIC INSTRUMENT
General & Plastic Surgery
110d
Cleared
Jan 21, 2010
ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENT
General & Plastic Surgery
113d
Cleared
Jun 18, 2009
ARAGON SURGICAL RF SYSTEM L2 INSTRUMENT
General & Plastic Surgery
132d
Cleared
Oct 31, 2008
ARAGON ONESHOT SYSTEM
General & Plastic Surgery
175d
Cleared
Jan 11, 2008
MODIFICATION TO: ARAGON SURGICAL LAPCAP
Obstetrics & Gynecology
32d
Cleared
May 30, 2007
ARAGON SURGICAL LAPCAP
Obstetrics & Gynecology
82d