Joimax GmbH - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Joimax GmbH has 7 FDA 510(k) cleared medical devices. Based in Los Gatos, US.
Last cleared in 2021. Active since 2005. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Joimax GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Joimax GmbH
7 devices
Cleared
Sep 01, 2021
EndoLIF Delta-Cage and DoubleWedge-Cage
Orthopedic
335d
Cleared
Jul 30, 2020
Joimax Intracs System
Orthopedic
309d
Cleared
Dec 18, 2019
Percusys® Plus Pedicle Screw System
Orthopedic
83d
Cleared
Apr 21, 2017
joimax Endovapor 2
General & Plastic Surgery
74d
Cleared
Nov 02, 2016
joimax Electrosurgical Instruments
General & Plastic Surgery
168d
Cleared
Jul 09, 2015
EndoLIF On-Cage
Orthopedic
71d
Cleared
Aug 12, 2005
JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS...
Orthopedic
37d