HomeUSAA Plus International, Inc.

A Plus International, Inc.

USA · Chino
✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 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
38listed device types
Class I 33Class II 4Class III 0unclassified 1
plus 40 registration records and 15 510(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
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 States40 registration records, 15 510(k), 0 PMA, 59 excluded
Brazil0 confirmed, 10 excluded
Saudi Arabia0 confirmed, 5 excluded
Canada0 confirmed, 4 excluded
Manufacturer names merged into this page: Premium Plus International Limited · A PLUS INTERNATIONAL, INC · HEALTH PLUS (SHANGHAI) INTERNATIONAL CO., LTD

Company information

Country
USA
City
Chino

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

71988
12003
12009
12010
12011
12016
22017
12022

FDA listed device types

showing 8 of 38
Gauze / Sponge,Nonresorbable For External Use 1Handpiece, Air-Powered, Dental 1Stool, Operating-Room 1Syringe, Restorative And Impression Material 1Toothbrush, Manual 1Shield, Nipple 1Absorber, Saliva, Paper 1Exerciser, Non-Measuring 1

Registration details (sample)

MarketIdentifierNameClass / date
USK213001Procedure Mask, Surgical Mask2022-05-11
USK170261Premium Plus Prophy Air Motor2017-10-19
USK163447Premium Plus Disposable Barrier Sleeve2017-06-20

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