Data / Medical devices / Germany / MedXpert GmbH
MedXpert GmbH: FDA-registered device maker in Eschbach Baden-Wurttemberg, Germany, 1 510(k) clearance
MedXpert GmbH is registered with the FDA (registration 3006801247) in Eschbach Baden-Wurttemberg, Germany. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 24, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006801247
- Address
- Max-Immelmann-Allee 19, Eschbach Baden-Wurttemberg, Germany, 79427
- Owner or operator
- MedXpert GmbH (10023342)
- Roles
- Specification developer
- First device listed
- November 19, 2007
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Instrument, Manual, Surgical, General Use | MDM | 1 | Specification developer | accessdata.fda.gov |
| Plate, Fixation, Bone | HRS | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 24, 2008 | K073556 | MEDXPERT P.E.S. (PECTUS EXACVATUM SYSTEM), MEDXPERT STRATOS | HRS | Substantially Equivalent | Medxpert GmbH | accessdata.fda.gov |
Compare with other makers
Updated June 24, 2008. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.