Galenica Enterprises, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Galenica Enterprises, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Galenica Enterprises, Inc. has 5 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 5 cleared submissions from 1984 to 1994. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Galenica Enterprises, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Galenica Enterprises, Inc.
5 devices
Cleared
Sep 08, 1994
LIGHTING SOURCE SYSTEM
Obstetrics & Gynecology
787d
Cleared
Dec 06, 1989
DISPOSABLE EXTERNAL CLAMPS
General & Plastic Surgery
30d
Cleared
Oct 18, 1988
DISPOSABLE AMNIOTOME
Obstetrics & Gynecology
75d
Cleared
Jun 13, 1986
GALENICA'S DISPOSABLE ANOSCOPES
Gastroenterology & Urology
87d
Cleared
Jul 31, 1984
VAGINAL SPECULUM - DISPOSABLE
Obstetrics & Gynecology
83d