Skip to the page

Data / Medical devices / Lamp, Surgical / Germany

FDA-registered makers of Lamp, Surgical in Germany: 8 establishments

8 establishments in Germany are registered with the FDA to make Lamp, Surgical (product code FTD). 2 have a 510(k) clearance or PMA approval on file and 0 have 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
Lamp, Surgical
Product code
FTD
Country
Germany

Makers of Lamp, Surgical in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Draegerwerk AG & Co. KGaALUEBECK Schleswig-Holstein, GermanyManufacturer1March 8, 2013000api.fda.gov
Stryker Leibinger GMBH & Co. KGFREIBURG Baden-Wurttemberg, GermanyContract manufacturer, Specification developer1June 30, 1998000api.fda.gov
Baxter Medical Systems GmbH + Co. KGMunich Bavaria, GermanySpecification developer0000api.fda.gov
Baxter Medical Systems GmbH + Co. KGSAALFELD Thuringia, GermanyComplaint file establishment, Manufacturer0000api.fda.gov
Dewimed Medizintechnik GMBHTUTTLINGEN Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Draeger Interservices GmbHLuebeck Schleswig-Holstein, GermanyContract manufacturer0000api.fda.gov
Inspital Medical Technology GMBHNeuss North Rhine-Westphalia, GermanyManufacturer0000api.fda.gov
PROVITA Medical GmbH & Co. KGWERMELSKIRCHEN North Rhine-Westphalia, 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.