Hollister, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hollister, Inc. - FDA 510(k) Cleared Devices
85
Total
78
Cleared
0
Denied
Hollister, Inc. has 78 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 78 cleared submissions from 1977 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Hollister, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hollister, Inc.
85 devices
Cleared
Apr 17, 2013
INSTAFLO BOWEL CATHETER SYSTEM KIT
Gastroenterology & Urology
128d
Cleared
Apr 22, 2010
INSTAFLO BOWEL CATHETER SYSTEM KIT
Gastroenterology & Urology
83d
Cleared
Aug 20, 2009
VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064,...
Gastroenterology & Urology
136d
Cleared
Feb 04, 2009
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007
Gastroenterology & Urology
103d
Cleared
Apr 12, 2005
EVADRI BLADDER CONTROL SYSTEMS
Gastroenterology & Urology
47d
Cleared
May 17, 2004
RESTORE WOUND CLEANSER
General & Plastic Surgery
52d
Cleared
Mar 19, 2002
INCARE PELVIC FLOOR THERAPY SYSTEM
Gastroenterology & Urology
134d
Cleared
Mar 05, 2002
INCARE PRESSURE BIOFEEDBACK VAGINAL PRESSURE PROBE AND ANAL PRESSURE PROBE
Gastroenterology & Urology
119d
Cleared
Jan 14, 2002
INCARE ADVANCE
Gastroenterology & Urology
87d
Cleared
Jan 07, 2002
INCARE INTERMITTENT CATHETER
Gastroenterology & Urology
90d
Cleared
Dec 19, 2001
MICROGYN PLUS STIMULATION DEVICE
Gastroenterology & Urology
90d
Cleared
Aug 15, 2001
AMEDA HYGIENIKIT
Obstetrics & Gynecology
90d
Looking for a specific device from Hollister, Inc.? Search by device name or K-number.
Search all Hollister, Inc. devices