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Data / Medical devices / Bandage, Elastic / Germany

FDA-registered makers of Bandage, Elastic in Germany: 14 establishments

14 establishments in Germany are registered with the FDA to make Bandage, Elastic (product code FQM). 0 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
Bandage, Elastic
Product code
FQM
Country
Germany

Makers of Bandage, Elastic in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
3M Deutschland GMBHKAMEN North Rhine-Westphalia, GermanyManufacturer0000api.fda.gov
3M Deutschland GmbHNeuss North Rhine-Westphalia, GermanySpecification developer0000api.fda.gov
BSN Medical GmbHHamburg, GermanyComplaint file establishment, Specification developer0000api.fda.gov
Bort GmbHWEINSTADT-BENZACH Baden-Wurttemberg, GermanyManufacturer0000api.fda.gov
Franz Kalff GMBHEuskirchen North Rhine-Westphalia, GermanySpecification developer0000api.fda.gov
Hans Hepp GMBH & Co. KGHAMBURG Lower Saxony, GermanyManufacturer0000api.fda.gov
KOB GmbHWolfstein Rhineland-Palatinate, GermanyContract manufacturer, Manufacturer0000api.fda.gov
Lohmann & Rauscher GMBH & Co. KGNEUWIED Rhineland-Palatinate, GermanyManufacturer, Specification developer0000api.fda.gov
Medi Se And Co. KGBAYREUTH Bavaria, GermanyManufacturer0000api.fda.gov
Paul Hartmann AGHeidenheim An Der Brenz Baden-Wurttemberg, GermanyForeign private label distributor, Specification developer0000api.fda.gov
RZ Medizintechnik GMBHTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Solventum Germany GmbHKamen North Rhine-Westphalia, GermanyExporter to the US, Manufacturer, Specification developer0000api.fda.gov
Symmetry Surgical GmbHTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
VBM Medizintechnik GMBHSULZ AM NECKAR Baden-Wurttemberg, 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.