Data / Medical devices / Ophthalmoscope, Battery-Powered / Germany
FDA-registered makers of Ophthalmoscope, Battery-Powered in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Ophthalmoscope, Battery-Powered (product code HLJ). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Ophthalmoscope, Battery-Powered
- Product code
- HLJ
- Country
- Germany
Makers of Ophthalmoscope, Battery-Powered in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Heine Optotechnik GMBH & Co. KG. | GILCHING Bavaria, Germany | Manufacturer | 4 | May 18, 2015 | 0 | 0 | 0 | api.fda.gov |
| Rudolf Riester GMBH | JUNGINGEN Baden-Wurttemberg, Germany | Manufacturer | 3 | July 24, 1995 | 0 | 0 | 0 | api.fda.gov |
| Carl Zeiss Meditec AG (jena) | JENA Thuringia, Germany | Specification developer | 1 | October 4, 1985 | 0 | 0 | 0 | api.fda.gov |
| Carl Zeiss Meditec AG (Jena) | Jena Thuringia, Germany | Manufacturer | 1 | October 4, 1985 | 0 | 0 | 0 | api.fda.gov |
| Kirchner & Wilhelm GmbH + Co.KG | Asperg Baden-Wurttemberg, Germany | Manufacturer | 1 | November 5, 2007 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.