HomeIndiaKIDS-E-DENTAL LLP

KIDS-E-DENTAL LLP

India · Mumbai Mah?R?Shtra
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Saudi Arabia, Singapore, Israel — 5 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
4listed device types
Class I 3Class II 1Class III 0
plus 4 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
4registered devices
Class II 4
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
3registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
3device registrations
CLASS B 3
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 States4 registration records, 1 510(k), 0 PMA, 5 excluded
Brazil4 confirmed, 0 excluded
Saudi Arabia3 confirmed, 0 excluded
Manufacturer names merged into this page: KIDS-E-DENTAL LLP · Kids-e-Dental LLP

Company information

Country
India
City
Mumbai Mah?R?Shtra

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

12024 · K240619

FDA listed device types

Maintainer, Space Preformed, Orthodontic 1Crown, Preformed 1Plier, Orthodontic 1Diammine Silver Fluoride Dental Hypersensitivity Varnish 1

Registration details (sample)

MarketIdentifierNameClass / date
USK240619e-SDF2024-03-06
BR82195309107Kids-e-CrownClass II
BR82195309108Bioflx CrownClass II
BR82195309109e-SDFClass II
SAME0000007621SFDAA00002Kids-e-Crown
SAME0000007621SFDAA00003e-space maintainer with accessories

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