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Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG

DE-MF-000012472 · Germany · Bingen am Rhein

Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 1 730 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa679
Class IIb1 051

Most frequent device types declared: 5.0 x 18.0mm K3Pro lmplant Drill (conical) - titanium, 5.0 x 3.0mm 0° Preform Abutment with 3mm Post - solid, 6.0 x 18.0mm K3Pro lmplant Drill (conical) - surgical steel, Drill sleeve 16mm for Drill 3.0mm, K3Pro XP Cover Screw Ø6,0mm x GH 3mm - 3mm Platform.

Among these devices, 101 are declared sterile, 298 implantable, 452 reusable.

Devices declared under this manufacturer

Showing 12 of 1 730 declared devices.

Catalogue references include BH3016, EAK 500030.VH/3Pro, KKB6.0/18OS, KRB5.0/18OS, MB.LK_1.6/3PRO, MU.XP 402010/2.SET.

European nomenclature codes declared: P01020101, Q010399, P0180, Q0199, P010299.

United States market access

FDA establishment registerRegistered with FDA
Matched entryARGON MEDICAL PRODUCTIONS & VERTRIEBS GESELLSCHAFT MBH & CO. (DE) · FDA 3011575197
Devices in EUDAMED1 730
Country of registrationGermany

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: United States only. Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG is registered in the United States but was not found in the Canadian register.

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