Covidien Lp, Formerly Registered AS United States is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Covidien Lp, Formerly Registered AS United States - FDA 510(k) Cleare...
7
Total
7
Cleared
0
Denied
Covidien Lp, Formerly Registered AS United States has 7 FDA 510(k) cleared medical devices. Based in North Haven, US.
Historical record: 7 cleared submissions from 2008 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Covidien Lp, Formerly Registered AS United States Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Covidien Lp, Formerly Registered AS United States
7 devices
Cleared
Sep 01, 2009
SILS CLINCHER, SILS DISSECTOR, SILS GRASPER, SILS L-HOOK, SILS SHEARS
General & Plastic Surgery
70d
Cleared
Jul 16, 2009
ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE
General & Plastic Surgery
21d
Cleared
Apr 10, 2009
AUTOSUTURE ENDO GIA STAPLERS WITH ENDO GIA SINGLE USE LOADING UNITS
General & Plastic Surgery
135d
Cleared
Mar 09, 2009
SILS STITCH ENDOSCOPIC SUTURING DEVICE
Gastroenterology & Urology
19d
Cleared
Nov 07, 2008
SILS PORT, MODELS SILSPT5, SILSPT12
General & Plastic Surgery
59d
Cleared
Sep 19, 2008
MODIFIED ENDO STICH
Gastroenterology & Urology
7d
Cleared
May 23, 2008
AUTOSUTURE VERSAPORT PLUS BLADLESS TROCAR
General & Plastic Surgery
29d