Data / Medical devices / Germany / WHR Hossinger Kunststofftechnik GMBH
WHR Hossinger Kunststofftechnik GMBH: FDA-registered device maker in Roding Bavaria, Germany, 1 510(k) clearance
WHR Hossinger Kunststofftechnik GMBH is registered with the FDA (registration 3010106508) in Roding Bavaria, Germany. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 10, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010106508
- Address
- Robert-Bosch-Str.1, Roding Bavaria, Germany, 93426
- Owner or operator
- whr Hossinger Kunststofftechnik GmbH (10043897)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- April 3, 2013
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Nasal, Oxygen | CAT | 1 | Contract manufacturer | accessdata.fda.gov |
| Light, Operating, Dental | EAZ | 1 | Contract manufacturer | accessdata.fda.gov |
| Orthopedic Manual Surgical Instrument | LXH | 1 | Contract manufacturer | accessdata.fda.gov |
| Rod, Fixation, Intramedullary And Accessories | HSB | 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 |
|---|---|---|---|---|---|---|
| October 10, 2013 | K131365 | T2 TIBIAL NAILING SYSTEM | HSB | Substantially Equivalent | Stryker Trauma AG | accessdata.fda.gov |
Compare with other makers
- All makers of Cannula, Nasal, Oxygen
- All makers of Rod, Fixation, Intramedullary And Accessories
- All makers of Light, Operating, Dental
- All makers of Orthopedic Manual Surgical Instrument
Updated October 10, 2013. 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.