HomeUSATri-Tech, Inc.

Tri-Tech, Inc.

USA · Mchenry
✓ 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
25listed device types
Class I 19Class II 5Class III 0unclassified 1
plus 26 registration records and 11 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
7registered devices
Class I 7
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 States26 registration records, 11 510(k), 0 PMA, 27 excluded
Brazil7 confirmed, 0 excluded
Saudi Arabia0 confirmed, 2 excluded
Canada0 confirmed, 1 excluded
Manufacturer names merged into this page: TRI-TECH FORENSICS, INC. · TRI-TECH MEDICAL, INC. · TRI-TECH FORENSICS, INC

Company information

Country
USA
City
Mchenry

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

11981
11985
11990
41991
11993
11994
11995
11997

FDA listed device types

showing 8 of 25
Tray, Blood Collection 1Bottle, Collection, Vacuum 1Regulator, Vacuum 1Oxygen Administration Kit 1Tubes, Vials, Systems, Serum Separators, Blood Collection 1Stretcher, Hand-Carried 1Container, Specimen, Sterile 1Regulator, Pressure, Gas Cylinder 1

Registration details (sample)

MarketIdentifierNameClass / date
USK971111TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER1997-06-16
USK952246TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KIT1995-06-20
USK922343TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT1994-02-17
BR80469670030Talas de Tração SlishmanClass I
BR80469670031FASPLINT tala para extremidadesClass I
BR80469670032FASPLINT com bolsa para tranporteClass I

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