HomeUSAAtlas Medical Products, Inc.

Atlas Medical Products, Inc.

USA · Hialeah
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Brazil — 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
76listed device types
Class I 52Class II 23Class III 0unclassified 1
plus 66 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
3registered devices
Class II 3
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
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 States66 registration records, 3 510(k), 0 PMA, 13 excluded
Brazil3 confirmed, 1 excluded
Canada0 confirmed, 2 excluded
Manufacturer names merged into this page: ATLAS MEDICAL PRODUCTS LLC · ATLAS MEDICAL

Company information

Country
USA
City
Hialeah

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

11991 · K914100
12011 · K102760
12019 · K191099

FDA listed device types

showing 8 of 76
Cap, Surgical 1Gauze / Sponge,Nonresorbable For External Use 1Container, Specimen, Sterile 1Azo-Dyes, Colorimetric, Bilirubin & Its Conjugates (Urinary, Non-Quant.) 1Test, Luteinizing Hormone (Lh), Over The Counter 1Circuit, Breathing (W Connector, Adaptor, Y Piece) 1Appliance, Colostomy, Disposable 1Solvent, Adhesive Tape 1

Registration details (sample)

MarketIdentifierNameClass / date
USK191099Atlas Multi-Drugs Screening Test Cup, Atlas Multi-Drugs Screening Test Panel2019-10-03
USK102760ATLAS HOME PREGNANCY TEST (MIDSTREAM FORMAT) MODEL 701720012011-08-03
USK914100STETHOSCOPE1991-11-07
BR80113770010Família MaternitestClass II
BR80113770011Família Strip Easy Test AlexdanClass II
BR80113770012Família Easy Test Plus AlexdanClass II

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