HomeBrazilAMERICA MEDTECH LTDA

AMERICA MEDTECH LTDA

Brazil
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, 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
19listed device types
Class I 1Class II 18Class III 0
plus 34 registration records and 48 510(k), 69 PMA
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
18registered devices
Class I 1Class II 17
23 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
1active device licences
Class III 1
29 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 States34 registration records, 48 510(k), 69 PMA, 102 excluded
Brazil18 confirmed, 36 excluded
Saudi Arabia0 confirmed, 6 excluded
Canada1 confirmed, 15 excluded
Manufacturer names merged into this page: DORNIER MEDTECH AMERICA, INC. · DORNIER MEDTECH AMERICA · AMERICA MEDTECH LTDA

Company information

Country
Brazil

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

32002
12006
22007
22008
22009
12011
32012
42013
12014
32015
12016
22017
12018
32019
22020
12021
22022
12023
12024
22025

FDA listed device types

showing 8 of 19
Image-Intensified Fluoroscopic X-Ray System, Mobile 1System, X-Ray, Fluoroscopic, Image-Intensified 1Lithotriptor, Extracorporeal Shock-Wave, Urological 1Cystoscope And Accessories, Flexible/Rigid 1Bronchoscope (Flexible Or Rigid) 1Dislodger, Stone, Flexible 1Endoscopic Access Overtube, Gastroenterology-Urology 1Catheter, Ureteral, Gastro-Urology 1

Registration details (sample)

MarketIdentifierNameClass / date
USK251403Dornier Bi-Polar Electrode BIP12CLM Bipolar 12° Medium Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIP12CLL Bipolar 12° Large Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIP30CLM Bipolar 30° Medium Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIP30CLL Bipolar 30° Large Cutting Loop 24 Fr Electrode-Sterile, Single-Use BIPMBLA Bipolar Medium Bladder Loop 24 Fr Electrode-Sterile, Single-Use BIPNEEL Bipolar Needle 24 Fr Electrode-Sterile, Single-Use BIPDDSC Bipolar Disc )2025-12-05
USK243820Hoover Negative Pressure Access Sheath (Hoover) (Hoover Model #'s IVX-NS-1040, IVX-NS-1050, IVX-NS-1140, IVX-NS-1150, IVX-NS-1240, IVX-NS-12502025-01-31
USK233380TRIDENT Mobile Fluoroscopy System2024-06-26
BR10183339002CÂNULAS DE LUZ CIRURGICA DORNIER REUTILIZÁVEISClass II
BR10302869013Fio Guia DornierClass II
BR80518279014CÂNULA DE LUZ CIRÚRGICA DESCARTÁVEL DORNIERClass II
CA65085EPOS ULTRAClass III

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