Medical Device Manufacturer · US , Palm Desert , CA

Nexmed, Inc. - FDA 510(k) Cleared Devices

6 submissions · 5 cleared · Since 1995
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
1–6 of 6
NEXFLEX TOTAL HIP SYSTEM
K033580 · LPH Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented · Orthopedic
Aug 2004 266d
NEXFLEX TOTAL KNEE SYSTEM
K991882 · JWH Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer · Orthopedic
Dec 1999 189d
NEXFLEX FEMORAL STEM, STANDARD DESIGN
K955170 · LPH Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented · Orthopedic
Feb 1996 88d
NEXLOCK FEMORAL STEM
K955171 · JDG Prosthesis, Hip, Femoral Component, Cemented, Metal · Orthopedic
Feb 1996 88d
NEXFLEX TOTAL HIP SYSTEM
K952629 · JDI Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented · Orthopedic
Sep 1995 92d
NEXMED CANCELLOUS BONE SCREWS
K951656 · HWC Screw, Fixation, Bone · Orthopedic
Jul 1995 99d
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