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Intl. Products, Inc.

USA · Vienna

✓ 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

16listed device types

Class I 14Class II 2Class III 0

plus 16 registration records and 9 510(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

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 States16 registration records, 9 510(k), 0 PMA, 43 excluded

Brazil0 confirmed, 6 excluded

Canada0 confirmed, 3 excluded

Manufacturer names merged into this page: CORE PRODUCTS INTL., INC. · LUNAPADS INTL. PRODUCTS LTD. · ELECTROMEDICAL PRODUCTS INTL., INC.

FDA 510(k) clearances by year

21980

11984

11990

21991

11993

11997

12005

FDA listed device types

showing 8 of 16

Joint, Knee, External Brace 1Orthosis, Lumbar 1Orthosis, Abdominal 1Orthosis, Truncal/Orthosis, Limb 1Shoe, Cast 1Splint, Hand, And Components 1Head Halter, Traction 1Massager, Therapeutic, Manual 1

Market	Identifier	Name	Class / date
US	K050600	MINILOC SAFETY INFUSION SET	2005-05-12
US	K963578	PC BASED ELECTROCARDIOGRAPH SYSTEM (PC-ECG)	1997-06-30
US	K931644	GERTIE MARX NEEDLE	1993-09-22

Intl. Products, 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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