Data / Medical devices / Germany / Kirchner & Wilhelm GmbH + Co.KG
Kirchner & Wilhelm GmbH + Co.KG: FDA-registered device maker in Asperg Baden-Wurttemberg, Germany, 1 510(k) clearance
Kirchner & Wilhelm GmbH + Co.KG is registered with the FDA (registration 8010427) in Asperg Baden-Wurttemberg, Germany. It lists 11 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 5, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8010427
- FEI number
- 6034
- Address
- Eberhardstrasse 56, Asperg Baden-Wurttemberg, Germany, 71679
- Owner or operator
- KIRCHNER and WILHELM GmbH (8010427)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- February 12, 1998
- Registered through
- 2026
- Brand names listed
- KaWe, KaWe LED head light H-800, KaWe MedCenter® 5000, KaWe binocular loupes, KaWe laryngoscope, KaWe ophthalmoscope, KaWe otoscope, KaWe specula and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Aid, Vision, Optical, Ac-Powered | HPI | 1 | Manufacturer | accessdata.fda.gov |
| Fork, Tuning | GWX | 1 | Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Headlamp, Operating, Battery-Operated | HPP | 1 | Manufacturer | accessdata.fda.gov |
| Laryngoscope, Rigid | CCW | 1 | Manufacturer | accessdata.fda.gov |
| Loupe, Binocular, Low Power | HJH | 1 | Manufacturer | accessdata.fda.gov |
| Loupe, Diagnostic/Surgical | FSP | 1 | Manufacturer | accessdata.fda.gov |
| Ophthalmoscope, Battery-Powered | HLJ | 2 | Manufacturer | accessdata.fda.gov |
| Otoscope | ERA | 1 | Manufacturer | accessdata.fda.gov |
| Percussor | GWZ | 1 | Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Specula Accessories | FXG | 1 | Manufacturer | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | 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 5, 2007 | K070270 | PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36 | HLJ | Substantially Equivalent | Kirchner & Wilhelm GmbH + Co.Kg | accessdata.fda.gov |
Compare with other makers
- All makers of Otoscope
- All makers of Stethoscope, Manual
- All makers of Specula Accessories
- All makers of Fork, Tuning
- All makers of Loupe, Diagnostic/Surgical
- All makers of Headlamp, Operating, Battery-Operated
Updated November 5, 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.