Data / Medical devices / Germany / Haselmeier GMBH
Haselmeier GMBH: FDA-registered device maker in STUTTGART Baden-Wurttemberg, Germany, 1 510(k) clearance
Haselmeier GMBH is registered with the FDA (registration 3007193283) in STUTTGART Baden-Wurttemberg, Germany. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 21, 2007. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3007193283
- Address
- Schelmenwasenstrasse 14, STUTTGART Baden-Wurttemberg, Germany, 70567
- Owner or operator
- HASELMEIER GMBH (9050535)
- Roles
- Specification developer
- First device listed
- December 17, 2007
- Registered through
- 2026
- Brand names listed
- HASELMEIER PEN
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Syringe, Piston | FMF | 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 |
|---|---|---|---|---|---|---|
| March 21, 2007 | K070100 | HASELMEIER PEN | FMF | Substantially Equivalent | Haselmeier Sarl | accessdata.fda.gov |
Compare with other makers
Updated March 21, 2007. 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.