Medovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medovations, Inc. - FDA 510(k) Cleared Devices
31
Total
31
Cleared
0
Denied
Medovations, Inc. has 31 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 31 cleared submissions from 1983 to 2015. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medovations, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medovations, Inc.
31 devices
Cleared
Mar 10, 2015
BULLDOG BIOPSY VALVE, OLYMPUS AND FUJINON
Gastroenterology & Urology
223d
Cleared
Nov 01, 2000
MEDOVATIONS ESOPHAGEAL DILATOR
Gastroenterology & Urology
90d
Cleared
Feb 02, 1998
MALONEY BOUGE (1210-XX)/HURST BOUGIE (1212-XX)
Gastroenterology & Urology
242d
Cleared
Dec 05, 1994
OVER THE GUIDEWIRE DILATATION SYSTEM
Gastroenterology & Urology
812d
Cleared
Dec 16, 1991
TROCAR CATHETER
General & Plastic Surgery
119d
Cleared
Dec 19, 1990
YANKAUER SUCTION DEVICE
General & Plastic Surgery
13d
Cleared
Dec 07, 1987
URETHAL CATHETER
Gastroenterology & Urology
48d
Cleared
Oct 14, 1987
STOMACH EVACULATOR - EWALD STYLE
Gastroenterology & Urology
296d
Cleared
Feb 19, 1987
OBERTO MOUTH PROP
Neurology
59d
Cleared
Jan 20, 1987
5 - IN - 1 CONNECTOR
General Hospital
29d
Cleared
Jan 23, 1986
ENTERAL FEEDING BAG
Gastroenterology & Urology
66d
Cleared
Jun 05, 1985
CHEST CATHETERS/THORACIC CATHETERS
General & Plastic Surgery
83d