Joimax GmbH
Joimax GmbH holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2021.
Top product codes for Joimax GmbH
Recent clearances by Joimax GmbH
- K203014 — EndoLIF Delta-Cage and DoubleWedge-Cage
- K192663 — Joimax Intracs System
- K192680 — Percusys® Plus Pedicle Screw System
- K170358 — joimax Endovapor 2
- K161378 — joimax Electrosurgical Instruments
- K151143 — EndoLIF On-Cage
- K051827 — JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPE
Data sourced from openFDA. This site is unofficial and independent of the FDA.