HomeUSARanir Corporation

Ranir Corporation

USA · Grand Rapids
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 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
14listed device types
Class I 12Class II 1Class III 0unclassified 1
plus 15 registration records and 9 510(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
4 including historic records
TWTaiwanTFDA
pendingnot queried
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 States15 registration records, 9 510(k), 0 PMA, 2 excluded
Saudi Arabia0 confirmed, 1 excluded
Manufacturer names merged into this page: RANIR LLC

Company information

Country
USA
City
Grand Rapids

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

12006
22009 · K091792
22010 · K102118
12011 · K103004
22012 · K120103
12013 · K133423

FDA listed device types

showing 8 of 14
Toothbrush, Powered 1Wax, Dental, Intraoral 1Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Non-Sterile 1Mirror, Mouth 1Instrument, Hand, Calculus Removal 1Floss, Dental 1Toothbrush, Manual 1Scraper, Tongue 1

Registration details (sample)

MarketIdentifierNameClass / date
USK133423REST ASSURED EXTRA COMFORT NITE PROTECTOR2013-12-20
USK120103REST ASSURED GENERATION III DENTAL PROTECTOR2012-02-03
USK112879REST ASSURED READY TO WEAR NITE PROTECTOR2012-01-27

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