Nexmed, Inc. - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
Nexmed, Inc. has 5 FDA 510(k) cleared medical devices. Based in Palm Desert, US.
Historical record: 5 cleared submissions from 1995 to 2004. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Nexmed, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Aug 05, 2004
NEXFLEX TOTAL HIP SYSTEM
Orthopedic
266d
Cleared
Dec 08, 1999
NEXFLEX TOTAL KNEE SYSTEM
Orthopedic
189d
Cleared
Feb 09, 1996
NEXFLEX FEMORAL STEM, STANDARD DESIGN
Orthopedic
88d
Cleared
Feb 09, 1996
NEXLOCK FEMORAL STEM
Orthopedic
88d
Cleared
Sep 08, 1995
NEXFLEX TOTAL HIP SYSTEM
Orthopedic
92d
Cleared
Jul 18, 1995
NEXMED CANCELLOUS BONE SCREWS
Orthopedic
99d