HomeGermanyYETI DENTALPRODUKTE GMBH

YETI DENTALPRODUKTE GMBH

Germany · Engen Baden-Wurttemberg
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Russia — 3 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
5listed device types
Class I 3Class II 2Class III 0
plus 5 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
5registered devices
Class II 5
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
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
8active registrations
Class 1 1Class 2a 7
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 States5 registration records, 1 510(k), 0 PMA, 1 excluded
Brazil5 confirmed, 0 excluded
Manufacturer names merged into this page: YETI DENTALPRODUKTE GMBH

Company information

Country
Germany
City
Engen Baden-Wurttemberg

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 510(k) clearances by year

12018 · K173971

FDA listed device types

Alloy, Metal, Base 1Powder, Porcelain 1Material, Impression Tray, Resin 1Wax, Dental, Intraoral 1Mirror, Mouth 1

Registration details (sample)

MarketIdentifierNameClass / date
USK173971K2 Zirkon Blank white classic; K2 Zirkon Blank translucent; K2 Blanks extreme translucent2018-11-15
BR80476699005Liga Metálica Odontológica SOLIDUR / SOLIBONDClass II
BR81196069009solibond nClass II
BR81196069012K2 HF CERÂMICA YETIClass II

Similar companies

1st German Health Resilience Conference
Germany · markets 0
3B Scientific GmbH
Germany · markets 1
3R LifeScience GmbH
Germany · markets 0
6th International Sports Pharmacy Symposium
Germany · markets 0
A&D Verpackungsmaschinenbau GmbH
Germany · markets 0
A. u. K. Müller GmbH & Co. KG
Germany · markets 0
Is this your company? Claim the page, add information or report a data error.Claim / report an error →