HomeUSABeyes Dental Canada, Inc.

Beyes Dental Canada, Inc.

USA · Dover
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Saudi Arabia, Canada — 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
40listed device types
Class I 30Class II 9Class III 0unclassified 1
plus 43 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
8registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
26 including historic records
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
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 States43 registration records, 2 510(k), 0 PMA
Saudi Arabia8 confirmed, 0 excluded
Manufacturer names merged into this page: BEYES DENTAL INC · BEYES DENTAL INC. · Beyes Dental Canada Inc.
Same-named companies — This database also contains companies with near-identical names: BEYES DENTAL INC.. Company name alone cannot separate their registrations, so the figures below may include either.

Company information

Country
USA
City
Dover

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

22011 · K112869

FDA listed device types

showing 8 of 40
Handpiece, Air-Powered, Dental 1Unit, Operative Dental 1Unit, Suction Operatory 1Syringe, Restorative And Impression Material 1Chair, Dental, Without Operative Unit 1Absorber, Saliva, Paper 1Handpiece, Contra- And Right-Angle Attachment, Dental 1Dam, Rubber 1

Registration details (sample)

MarketIdentifierNameClass / date
USK112869EASYPROPHY SERIES AIR POLISH DEVICES, MODELS EASYPROPHY 200 AND EASYPROPHY 4002011-12-16
USK112623AIRLIGHT DENTAL HANDPIECE2011-12-16
SAME0000011395SFDAA00004SLIMAX–C Plus®
SAME0000011395SFDAA00010CareMaster®

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