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Lifeward GmbH

✓ Record-verifiedregistrations found in 4 marketsEU SRN IL-MF-000033442

This company has registrations in European Union, United States, United Kingdom, Australia — 4 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

15UDI-DI device records

Class I 13Class IIa 2

USUnited StatesFDA openFDA

2listed device types

Class I 1Class II 1Class III 0

plus 13 registration records and 0 510(k)

UKUnited KingdomMHRA PARD

2registered device records

Class I 1Class IIa 1

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

1active ARTG entries

Class I 1

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.

European Union15 raw hits, 0 excluded, 15 confirmed

United States13 registration records, 0 510(k), 0 PMA, 1 excluded

United Kingdom2 confirmed, 0 excluded

Manufacturer names merged into this page: Lifeward LTD. · LIFEWARD, INC.

Regulatory identity

EU manufacturer SRN: IL-MF-000033442
EU authorised representative: MedNet EC-REP GmbH
UK responsible person: SportsMed Products Limited

Registration details (sample)

Market	Identifier	Name	Class / date
EU	00860001744514	ReWalk 7	Class IIa
EU	00861803000303	ReWalK P6.0	Class IIa
EU	00850022788260	—	Class I
EU	00850022788253	—	Class I
UK	61495	AlterG	Class I
UK	58943	Restore System	Class IIa

Lifeward GmbH

Registrations by market

How these numbers were verified

Regulatory identity

Company information

FDA listed device types

Registration details (sample)

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