Data / Medical devices / Germany / Vepro AG
Vepro AG: FDA-registered device maker in PFUNGSTADT Hesse, Germany, 1 510(k) clearance
Vepro AG is registered with the FDA (registration 9614981) in PFUNGSTADT Hesse, Germany. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 19, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9614981
- FEI number
- 3004562407
- Address
- Max-Planck STR. 1-3, PFUNGSTADT Hesse, Germany, 64319
- Owner or operator
- VEPRO AG (9030770)
- Roles
- Manufacturer
- First device listed
- October 31, 2008
- Registered through
- 2026
- Brand names listed
- EMR Manager
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| November 19, 1997 | K972215 | MEDIMAGE | LLZ | Substantially Equivalent | Vepro - Computersysteme GmbH | accessdata.fda.gov |
Compare with other makers
Updated November 19, 1997. 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.