O.R. Resources, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
O.R. Resources, Inc. - FDA 510(k) Cleared Devices
4
Total
3
Cleared
0
Denied
O.R. Resources, Inc. has 3 FDA 510(k) cleared medical devices. Based in Annapolis, US.
Historical record: 3 cleared submissions from 1994 to 1995. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by O.R. Resources, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - O.R. Resources, Inc.
4 devices
Cleared
Sep 08, 1995
EXUSORB STERILE ABSORBENT
General & Plastic Surgery
64d
Cleared
May 12, 1995
HYDROGEL DRESSING
General & Plastic Surgery
198d
Cleared
Dec 05, 1994
SURE-FLO IRRIGATION Y TUBING SET
General & Plastic Surgery
104d
Cleared
Apr 19, 1994
SURE-FLO INSUFFLATION TUBING
Obstetrics & Gynecology
433d