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Data / Medical devices / Rongeur, Manual / Germany

FDA-registered makers of Rongeur, Manual in Germany: 19 establishments

19 establishments in Germany are registered with the FDA to make Rongeur, Manual (product code HAE). 6 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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Get makers of this device in GermanyWatch these makers
Device
Rongeur, Manual
Product code
HAE
Country
Germany

Makers of Rongeur, Manual in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Morpheus AGSpaichingen Baden-Wurttemberg, GermanyManufacturer2March 3, 2023000api.fda.gov
Aesculap AGTUTTLINGEN, DONAU Baden-Wurttemberg, GermanyManufacturer1June 29, 2023000api.fda.gov
FEHLING INSTRUMENTS GmbHKARLSTEIN Bavaria, GermanyManufacturer1August 4, 2016000api.fda.gov
Geister Medizintechnik GMBHTUTTLINGEN Baden-Wurttemberg, GermanyManufacturer1June 6, 2025000api.fda.gov
Tontarra Medizintechnik GMBHWURMLINGEN Baden-Wurttemberg, GermanyContract manufacturer, Manufacturer1September 15, 2026000api.fda.gov
Vitalitec International Medizintechnik GmbHBALGHEIM Baden-Wurttemberg, GermanySpecification developer1June 18, 2016000api.fda.gov
BAK KOHLER Medical KGNEUHAUSEN OB ECK-Schwandorf Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
EFINGER INSTRUMENTS GmbH & Co. KGSPAICHINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Fetzer Medical GMBH & Co.kgTuttlingen Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
FRITZ HUBER GmbH & Co. KGTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Kapp Surgical GMBHDUERBHEIM Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
KLS Martin SE & Co. KGMuhlheim/Donau Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Koscher & Wuertz GMBHSPAICHINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Max Hauser Suddeutsche Chirurgiemechanik GMBHTUTTLINGEN Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
PROMOTEC-MEDIZINTECHNIK GmbHBlankenfelde / Mahlow Brandenburg, GermanyContract manufacturer0000api.fda.gov
Raimund Wenzler GMBH, Instrumenten-ManufakturBALGHEIM Baden-Wurttemberg, GermanyContract manufacturer, Manufacturer0000api.fda.gov
Rominger Medizintechnik GMBHSEITINGEN-OBERFLACHT Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
S.U.A. Martin GMBH & Co.RIETHEIM-WEILHEIM Baden-Wurttemberg, GermanyContract manufacturer, Manufacturer0000api.fda.gov
Tekno Medical Optik-Chirurgie GMBHTUTTLINGEN-Nendingen Baden-Wurttemberg, GermanyContract manufacturer0000api.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.