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Data / Medical devices / Biomicroscope, Slit-Lamp, Ac-Powered / Germany

FDA-registered makers of Biomicroscope, Slit-Lamp, Ac-Powered in Germany: 7 establishments

7 establishments in Germany are registered with the FDA to make Biomicroscope, Slit-Lamp, Ac-Powered (product code HJO). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. 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.

Device
Biomicroscope, Slit-Lamp, Ac-Powered
Product code
HJO
Country
Germany

Makers of Biomicroscope, Slit-Lamp, Ac-Powered in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Carl Zeiss Meditec AG (jena)JENA Thuringia, GermanySpecification developer10August 24, 2018000api.fda.gov
Carl Zeiss Meditec AG (Jena)Jena Thuringia, GermanyManufacturer9May 31, 2017030api.fda.gov
Carl Zeiss Vision GMBHAALEN Baden-Wurttemberg, GermanyComplaint file establishment, Exporter to the US, Specification developer2March 18, 2026000api.fda.gov
CARL ZEISS MEDITEC AG (Munich)Muenchen Bavaria, GermanyManufacturer1September 9, 2014000api.fda.gov
Carl Zeiss Meditec AG (oberkochen)OBERKOCHEN Baden-Wurttemberg, GermanyManufacturer1February 23, 2017000api.fda.gov
Karl Storz Se & Co KGTUTTLINGEN Baden-Wurttemberg, GermanySpecification developer0000api.fda.gov
Oculus Optikgerate GMBHWETZLAR Hesse, GermanyManufacturer0000api.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.