Geritrex Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Geritrex Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Geritrex Corp. has 4 FDA 510(k) cleared medical devices. Based in Mount Vernon, US.
Historical record: 4 cleared submissions from 1993 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Geritrex Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Geritrex Corp.
4 devices
Cleared
Apr 03, 1995
GRX FOAM DRESSING
General & Plastic Surgery
159d
Cleared
Sep 22, 1994
GERITREX STERILE SALINE SOLUTION FOR IRRIGATION
General Hospital
545d
Cleared
Feb 14, 1994
GERITREX STERILE WATER FOR IRRIGATION
General Hospital
325d
Cleared
Jul 13, 1993
GERITREX STERILE SALINE WET DRESSING
General & Plastic Surgery
109d