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Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG

Germany · Bingen Am Rhein

✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

n/aThis registry lists domestic registrants only

EUEuropean UnionEUDAMED

pendingnot queried

USUnited StatesFDA openFDA

3listed device types

Class I 0Class II 3Class III 0

plus 4 registration records and 4 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

0registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

0active device licences

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

pendingnot queried

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

pendingnot queried

RURussiaRoszdravnadzor

pendingnot queried

Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States4 registration records, 4 510(k), 0 PMA, 6 excluded

Brazil0 confirmed, 2 excluded

Canada0 confirmed, 2 excluded

Manufacturer names merged into this page: ARGON MEDICAL PRODUCTIONS & VERTRIEBS GESELLSCHAFT MBH & CO.

Same-named companies — This database also contains companies with near-identical names: ARGON MEDICAL PRODUCTIONS & VERTRIEBS GESELLSCHAFT MBH & CO.. Company name alone cannot separate their registrations, so the figures below may include either.

FDA 510(k) clearances by year

12015 · K141159

12016 · K160574

12017 · K160581

12020 · K190192

FDA listed device types

Implant, Endosseous, Root-Form 1Sterilization Wrap Containers, Trays, Cassettes & Other Accessories 1Abutment, Implant, Dental, Endosseous 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K190192	K3Pro Konus New Abutments and Implants	2020-02-10
US	K160581	K3PRO Konus Additional Abutments and Implants	2017-03-24
US	K160574	K3PRO SURGICAL TRAY	2016-12-20

Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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