Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Joimax GmbH with 7 510(k) clearances. The most recent is a 510(k) clearance dated Sep 1, 2021: EndoLIF Delta-Cage and DoubleWedge-Cage.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Sep 1, 2021 | EndoLIF Delta-Cage and DoubleWedge-CageK203014 · MAX | 510(k) clearances |
| Jul 30, 2020 | Joimax Intracs SystemK192663 · OLO | 510(k) clearances |
| Dec 18, 2019 | Percusys® Plus Pedicle Screw SystemK192680 · NKB | 510(k) clearances |
| Apr 21, 2017 | joimax Endovapor 2K170358 · GEI | 510(k) clearances |
| Nov 2, 2016 | joimax Electrosurgical InstrumentsK161378 · GEI | 510(k) clearances |
| Jul 9, 2015 | EndoLIF On-CageK151143 · MAX | 510(k) clearances |
| Aug 12, 2005 | JOIMAX ENDOSCOPE/MULTISCOPE, THESSYS FORAMINOSCOPE/MULTISCOPE, THESSYS LAMINOSCOPE/MULTISCOPEK051827 · HRX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
