HomeGermanyRENFERT GMBH.

RENFERT GMBH.

Germany · Hilzingen Baden-Wurttemberg
✓ Record-verifiedregistrations found in 7 markets

This company has registrations in United States, Brazil, Saudi Arabia, Taiwan, Australia, Israel, Russia — 7 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 3Class II 0Class III 0
plus 3 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class I 2
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
5registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
9valid device licences
Class I 9
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
5active ARTG entries
Class I 5
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
3registrations
RURussiaRoszdravnadzor
31active registrations
Class 1 19Class 2a 12
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 States3 registration records, 0 510(k), 0 PMA
Brazil2 confirmed, 0 excluded
Saudi Arabia5 confirmed, 0 excluded
Manufacturer names merged into this page: RENFERT GMBH · RENFERT GMBH. · Renfert GmbH

Company information

Country
Germany
City
Hilzingen 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 listed device types

Cleanser, Denture, Prescription 1Cleaner, Denture, Mechanical 1Amalgamator, Dental, Ac-Powered 1

Registration details (sample)

MarketIdentifierNameClass / date
BR81418590002help:ex plaque fClass I
BR81418590001help:ex plaque pClass I
SAME0000000707SFDAA00009help:ex
SAME0000000707SFDAA00008Sympro

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