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SHENZHEN LEAFLIFE TECHNOLOGY CO., LTD.

China · Shenzhen

✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Canada, Australia, Israel — 5 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

pendingnot queried

EUEuropean UnionEUDAMED

pendingnot queried

USUnited StatesFDA openFDA

5listed device types

Class I 1Class II 4Class III 0

plus 8 registration records and 7 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

4registered devices

Class II 4

5 including historic records

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

pendingnot queried

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

1active ARTG entries

IIb 1

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 States8 registration records, 7 510(k), 0 PMA

Brazil4 confirmed, 0 excluded

Manufacturer names merged into this page: SHENZHEN LEAFLIFE TECHNOLOGY CO., LTD.

FDA 510(k) clearances by year

12020 · K202980

12021 · K212697

12022 · K220103

12023 · K230362

12024 · K233760

22025 · K253219

FDA listed device types

Low Power Electrosurgical Devices For Skin Lesion Destruction 1Massager, Vacuum, Radio Frequency Induced Heat 1Powered Laser Surgical Instrument 1Light Based Over-The-Counter Hair Removal 1Massager, Therapeutic, Electric 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K253219	LeafPure-Echo (LM-LPNdA)	2025-11-25
US	K250916	WinForth (LM-E470KA)	2025-08-14
US	K233760	Mjolnir Pro. (Multielectrode plasma)	2024-02-20
BR	82149139005	Mjolnir Pro	Class II
BR	80451969015	Rennova Diamond Tech	Class II
BR	80580299002	EuroPlasma	Class II

SHENZHEN LEAFLIFE TECHNOLOGY CO., 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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