Data / Medical devices / Applicator, Ent / Germany

FDA-registered makers of Applicator, Ent in Germany: 19 establishments

Name: FDA-registered makers of Applicator, Ent in Germany
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

19 establishments in Germany are registered with the FDA to make Applicator, Ent (product code KCJ). 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: Applicator, Ent
Product code: KCJ
Country: Germany

Makers of Applicator, Ent in Germany

Maker	Location	Role	Source
Aesculap AG	TUTTLINGEN, DONAU Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Asanus Medizintechnik GMBH	NEUHAUSEN OBECK Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler, Specification developer	api.fda.gov
Bauer Und Haselbarth-Chirurg GMBH	ELLERAU Schleswig-Holstein, Germany	Contract manufacturer, Manufacturer	api.fda.gov
Dimeda Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Dausch Medizintechnik GmbH	WURMLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Evonos GMBH & Co. KG	Tuttlingen Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Fetzer Medical GMBH & Co.kg	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Hafner Chirurgische Instrumente	BALGHEIM Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
HGR Instrumente GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
JR Montagearbeiten	TUTTLINGEN Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
KLS Martin Se & Co. KG	Fridingen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
KLS Martin SE & Co. KG	Muhlheim/Donau Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Mattes Instrumente GMBH	Tuttlingen-Nendingen Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
Med2b Ltd.	Kitzingen Bavaria, Germany	Manufacturer	api.fda.gov
Medicon, E.G.	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Richard Wolf GMBH	KNITTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Rommelag CDMO GmbH	Sulzbach-Laufen Baden-Wurttemberg, Germany	Contract manufacturer	api.fda.gov
Tekno Medical Optik-Chirurgie GMBH	TUTTLINGEN-Nendingen Baden-Wurttemberg, Germany	Manufacturer, Repackager or relabeler	api.fda.gov
Teufel & Gerlach GmbH	Tuttlingen Baden-Wurttemberg, Germany	Contract manufacturer	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.