Generic Medical Device, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Generic Medical Device, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Generic Medical Device, Inc. has 4 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 4 cleared submissions from 2007 to 2011. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Generic Medical Device, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Generic Medical Device, Inc.
4 devices
Cleared
Jun 30, 2011
GMD UNIVERSAL URINARY INCONTINENCE SLING
Gastroenterology & Urology
59d
Cleared
Mar 03, 2009
GMD UNIVERSAL SLING, MODEL PRODUCT CODE 1010 AND 1020
Gastroenterology & Urology
99d
Cleared
Apr 27, 2007
UNIVERSAL SURGICAL MESH, MODEL 100
General & Plastic Surgery
114d
Cleared
Jan 17, 2007
GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200
Obstetrics & Gynecology
65d