Onux Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Onux Medical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Onux Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in Hampton, US.
Historical record: 5 cleared submissions from 2001 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Onux Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Onux Medical, Inc.
5 devices
Cleared
Dec 27, 2002
NON-BIOABSORBABLE STAPLE
General & Plastic Surgery
80d
Cleared
Nov 19, 2002
MANUAL TOUCHE SYSTEM
General & Plastic Surgery
90d
Cleared
Mar 08, 2002
SALUTE, MODEL 3022
General & Plastic Surgery
71d
Cleared
May 17, 2001
ENDOSCOPIC STAPLE REMOVAL INSTRUMENT
General & Plastic Surgery
77d
Cleared
Feb 13, 2001
SALUTE
General & Plastic Surgery
90d