Advanced Surgical Concepts is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Surgical Concepts - FDA 510(k) Cleared Devices
Recent clearances: Guardenia (GAR-1), PneumoLiner
9
Total
9
Cleared
0
Denied
Advanced Surgical Concepts has 9 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Last cleared in 2023. Active since 2007. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Advanced Surgical Concepts Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Advanced Surgical Concepts
9 devices
Cleared
Sep 29, 2023
Guardenia (GAR-1)
General & Plastic Surgery
24d
Cleared
Feb 25, 2020
PneumoLiner
Obstetrics & Gynecology
137d
Cleared
Sep 06, 2012
ASC QUADPORT + LAPAROSCOPIC ACCESS DEVICE
General & Plastic Surgery
128d
Cleared
Jan 18, 2012
TRIPORT, TRIPORT+, TRIPORT15, QUADPORT
General & Plastic Surgery
244d
Cleared
Jan 26, 2011
ASC TRIPORT+ LAPAROSCOPIC ACCESS DEVICE
General & Plastic Surgery
23d
Cleared
Nov 29, 2010
ASC TRIPORT LAPAROSCOPIC ACCESS DEVICE MODEL TPRT-02-01 (WA58000T), ASC...
General & Plastic Surgery
154d
Cleared
Jan 29, 2008
ASC TRIPORT LAPAROSCOPIC ACCESS DEVICE
General & Plastic Surgery
29d
Cleared
Dec 03, 2007
R-PORT II LAPAROSCOPIC ACCESS DEVICE
General & Plastic Surgery
24d
Cleared
Aug 23, 2007
R-PORT LAPAROSCOPIC ACCESS DEVICE
General & Plastic Surgery
218d