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Forum Engineering Technologies, Ltd.

Israel · Rishon Lezion

✓ 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

3listed device types

Class I 2Class II 0Class III 0unclassified 1

plus 5 registration records and 3 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

2registered devices

Class I 1Class II 1

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

1 including historic records

TWTaiwanTFDA

0valid device licences

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 States5 registration records, 3 510(k), 0 PMA, 1 excluded

Brazil2 confirmed, 0 excluded

Manufacturer names merged into this page: FORUM ENGINEERING TECHNOLOGIES (96) LTD.

Same-named companies — This database also contains companies with near-identical names: Forum Engineering Technologies (96) , Ltd.. Company name alone cannot separate their registrations, so the figures below may include either.

FDA 510(k) clearances by year

12011 · K111474

12013 · K121206

12024 · K232551

FDA listed device types

Locator, Root Apex 1Accessories, Implant, Dental, Endosseous 1Handpiece, Direct Drive, Ac-Powered 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K232551	EM-07 Cordless Endo Motor	2024-07-09
US	K121206	DETECT	2013-01-10
US	K111474	BINGO PRO	2011-11-02
BR	80082120009	NOVAPEX	Class II
BR	80745400048	Propex Pixi®	Class I

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Forum Engineering Technologies, Ltd.

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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