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TRI-TECH MEDICAL, INC.

USA · Avon

✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Saudi Arabia, Israel — 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

6listed device types

Class I 4Class II 2Class III 0

plus 6 registration records and 11 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

1registered 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

1registrations

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 States6 registration records, 11 510(k), 0 PMA, 28 excluded

Brazil0 confirmed, 1 excluded

Saudi Arabia1 confirmed, 1 excluded

Canada0 confirmed, 1 excluded

Manufacturer names merged into this page: TRI-TECH MEDICAL, INC. · tri m medical

FDA 510(k) clearances by year

11981

11985

11990

41991

11993

11994

11995

11997

FDA listed device types

Bottle, Collection, Vacuum 1Regulator, Vacuum 1Apparatus, Suction, Single Patient Use, Portable, Nonpowered 1Humidifier, Non-Direct Patient Interface (Home-Use) 1Regulator, Pressure, Gas Cylinder 1Flowmeter, Tube, Thorpe, Back-Pressure Compensated 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K971111	TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER	1997-06-16
US	K952246	TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KIT	1995-06-20
US	K922343	TRI-TECH INC. CUSTOM SEXUAL ASSAULT KIT	1994-02-17
SA	ME0000001806SFDAA00013	surgical pad	—

TRI-TECH MEDICAL, INC.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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