HomeUSAGEORGE TAUB PRODUCTS & FUSION CO., INC.

GEORGE TAUB PRODUCTS & FUSION CO., INC.

USA · Jersey City
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Israel — 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
21listed device types
Class I 13Class II 8Class III 0
plus 24 registration records and 2 510(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
2registrations
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, 2 510(k), 0 PMA, 1 excluded
Manufacturer names merged into this page: GEORGE TAUB PRODUCTS & FUSION CO., INC.

Company information

Country
USA
City
Jersey City

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

11984 · K833640
11986 · K854588

FDA listed device types

showing 8 of 21
Sealant, Pit And Fissure, And Conditioner 1Cement, Dental 1Liner, Cavity, Calcium Hydroxide 1External Cleaning Solution 1Coating, Filling Material, Resin 1Material, Tooth Shade, Resin 1Denture Preformed (Partially Prefabricated Denture) 1Denture Repair Kit 1

Registration details (sample)

MarketIdentifierNameClass / date
USK854588INSTA-GLAZE1986-02-04
USK833640HYDROXYLINE1984-02-27

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