Ethicon, Inc. - FDA 510(k) Cleared Devices
202
Total
195
Cleared
0
Denied
FDA 510(k) cleared devices by Ethicon, Inc. Obstetrics & Gynecology ✕
17 devices
Cleared
Sep 27, 2013
MORCELLEX SIGMA GENERATOR
Obstetrics & Gynecology
113d
Cleared
Jun 11, 2012
ARTISYN Y-SHAPED MESH
Obstetrics & Gynecology
224d
Cleared
Dec 02, 2011
VERSAPOINT II BIPOLAR ELECTROSURGERY GENERATOR, VERSAPOINT II 44MM ANGLED...
Obstetrics & Gynecology
163d
Cleared
Mar 24, 2010
GYNCARE MORCELLEX TISSUE MORCELLATOR
Obstetrics & Gynecology
51d
Cleared
May 15, 2008
GYNECARE PROLIFT +M* PELVIC FLOOR REPAIR SYSTEMS
Obstetrics & Gynecology
346d
Cleared
Feb 26, 2007
GYNECARE PROSIMA PELVIC FLOOR REPAIR SYSTEMS
Obstetrics & Gynecology
91d
Cleared
Jul 14, 2006
GYNECARE MORCELLEX TISSUE MORCELLATOR, MODELS MX0100 AND MX0100R
Obstetrics & Gynecology
88d
Cleared
Dec 22, 2004
GYNECARE PROLENE FASTENER SYSTEM
Obstetrics & Gynecology
89d
Cleared
Feb 07, 2000
GYNECARE LAPAROSCOPIC MORCELLATOR
Obstetrics & Gynecology
90d
Cleared
Jan 24, 2000
VERSAPOINT ELECTROSURGERY SYSTEM (SCUBA)
Obstetrics & Gynecology
26d
Cleared
Mar 11, 1994
ENDOPATH RELOADABLE LINEAR CUTTER
Obstetrics & Gynecology
381d
Cleared
Feb 03, 1992
DISPOSABLE TROCAR SLEEVE WITH DILATING OBTURATOR
Obstetrics & Gynecology
90d