Mednext, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Mednext, Inc. has 7 FDA 510(k) cleared medical devices. Based in West Point Beach, US.
Historical record: 7 cleared submissions from 1993 to 1998.
Browse the FDA 510(k) cleared devices submitted by Mednext, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Nov 06, 1998
TRITON HUDSON CHUCK ATTACHMENT
Neurology
64d
Cleared
Aug 20, 1997
MEDNEXT 1000 DRILL
General & Plastic Surgery
61d
Cleared
Feb 28, 1997
MEDNEXT SURGICAL BUR
Orthopedic
56d
Cleared
Aug 17, 1994
MEDNEXT MICRO-DRILL
Ear, Nose, Throat
49d
Cleared
May 03, 1994
MEDNEXT BUR
Neurology
151d
Cleared
Feb 22, 1994
MEDNEXT BUR
Ear, Nose, Throat
96d
Cleared
Jul 22, 1993
MEDNEXT 1000 BONE DISSECTING SYSTEM
Orthopedic
203d