HomeGermanymedmix Deutschland GmbH

medmix Deutschland GmbH

Germany · Kiel
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 2 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
9listed device types
Class I 3Class II 5Class III 0unclassified 1
plus 24 registration records and 0 510(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
3active device licences
Class II 3
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 States24 registration records, 0 510(k), 0 PMA, 4 excluded
Brazil0 confirmed, 2 excluded
Canada3 confirmed, 0 excluded
Manufacturer names merged into this page: medmix Deutschland GmbH · MEDMIX DEUTSCHLAND GMBH

Company information

Country
Germany
City
Kiel

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA listed device types

showing 8 of 9
Adhesive, Bracket And Tooth Conditioner, Resin 1Diammine Silver Fluoride Dental Hypersensitivity Varnish 1Varnish, Cavity 1Material, Tooth Shade, Resin 1Agent, Tooth Bonding, Resin 1Cord, Retraction 1Needle, Dental 1Syringe, Restorative And Impression Material 1

Registration details (sample)

MarketIdentifierNameClass / date
CA89662DENTAL INJECTION NEEDLESClass II
CA90721ENDO IRRIGATION NEEDLESClass II
CA93199SUCTION NEEDLESClass II

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