Joimax GmbH

7 FDA 510(k) medical device clearances.

Top product codes for Joimax GmbH

GEI — General, Plastic Surgery 2 devices
MAX — Orthopedic 2 devices
HRX — Orthopedic 1 device
NKB — Orthopedic 1 device
OLO — Neurology 1 device

Recent clearances by Joimax GmbH

K203014 — EndoLIF Delta-Cage and DoubleWedge-Cage MAX · 2021-09-01
K192663 — Joimax Intracs System OLO · 2020-07-30
K192680 — Percusys® Plus Pedicle Screw System NKB · 2019-12-18
K170358 — joimax Endovapor 2 GEI · 2017-04-21
K161378 — joimax Electrosurgical Instruments GEI · 2016-11-02
K151143 — EndoLIF On-Cage MAX · 2015-07-09
K051827 — JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPE HRX · 2005-08-12

Data sourced from openFDA. This site is unofficial and independent of the FDA.