Data / Medical devices / Germany / Weber Medical GMBH
Weber Medical GMBH: FDA-registered device maker in Lauenfoerde Lower Saxony, Germany, 1 510(k) clearance
Weber Medical GMBH is registered with the FDA (registration 3007165178) in Lauenfoerde Lower Saxony, Germany. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 11, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007165178
- Address
- Sohnreystrasse 4, Lauenfoerde Lower Saxony, Germany, 37697
- Owner or operator
- Weber Medical GmbH (10026908)
- Roles
- Manufacturer
- First device listed
- September 1, 2008
- Registered through
- 2026
- Brand names listed
- weberneedle®basic
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 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 |
|---|---|---|---|---|---|---|
| August 11, 2008 | K073352 | WEBERNEEDLE BASIC LASER | ILY | Substantially Equivalent | Weber Medical GmbH | accessdata.fda.gov |
Compare with other makers
Updated August 11, 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.