Surgiquest, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgiquest, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Surgiquest, Inc. has 9 FDA 510(k) cleared medical devices. Based in Orange, US.
Historical record: 9 cleared submissions from 2007 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Surgiquest, Inc. Filter by specialty or product code using the sidebar.
Surgiquest, Inc. — FDA 510(k) Products and Clearance History
9 devices
Cleared
Mar 20, 2015
SurgiQuest AirSeal iFS System
Obstetrics & Gynecology
112d
Cleared
Aug 22, 2013
SURGIQUEST AIRSEAL IFS
General & Plastic Surgery
38d
Cleared
Jul 03, 2012
MODIFIED SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM WITH INTEGRATED...
Obstetrics & Gynecology
61d
Cleared
May 25, 2011
SUGIQUEST AIRSEALOPTICAL TROCAR & CANNULA SYSTEM WITH INTEGRATED INSUFFLATOR...
Obstetrics & Gynecology
159d
Cleared
May 05, 2010
SURGIQUEST ANCHORPORT SIL KIT
General & Plastic Surgery
104d
Cleared
Nov 05, 2009
SURGIQUEST AIRSEAL OPTICAL TROCAR AND CANNULA SYSTEM
General & Plastic Surgery
83d
Cleared
Dec 15, 2008
AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM
General & Plastic Surgery
45d
Cleared
Jul 30, 2007
SURGIQUEST AIRSEAL OPTICAL TROCAR & CANNULA SYSTEM
General & Plastic Surgery
52d
Cleared
Mar 14, 2007
SURGIQUEST ELASTOMERIC OPTICAL TROCAR & CANNULA
General & Plastic Surgery
76d