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LIVSMED Co., Ltd.

✓ Record-verifiedregistrations found in 9 marketsEU SRN KR-MF-000011855

This company has registrations in European Union, United States, United Kingdom, Canada, Taiwan, Singapore, Australia, Hong Kong, Israel — 9 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

267UDI-DI device records

Class IIa 117Class IIb 150

USUnited StatesFDA openFDA

4listed device types

Class I 2Class II 2Class III 0

plus 9 registration records and 12 510(k)

UKUnited KingdomMHRA PARD

8registered device records

Class IIa 4Class IIb 4

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

4 including historic records

TWTaiwanTFDA

4valid device licences

Class II 4

SGSingaporeHSA SMDR

8device registrations

CLASS B 8

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

5active ARTG entries

IIa 3IIb 2

HKHong KongMDACS

5valid listings

Class II 3Class III 2

ILIsraelAMAR

2registrations

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 Union267 raw hits, 0 excluded, 267 confirmed

United States9 registration records, 12 510(k), 0 PMA

United Kingdom8 confirmed, 0 excluded

Manufacturer names merged into this page: LivsMed Inc. · LIVSMED INC.

Regulatory identity

EU manufacturer SRN: KR-MF-000011855
EU authorised representative: Meridius Medical Europe Limited
UK responsible person: Qserve Group UK, Ltd.
Exhibition record: CMEF 93rd (Apr 2026, Shanghai)

FDA 510(k) clearances by year

32020

22021 · K212500

12022 · K220384

32023 · K230498

22024 · K241138

12025 · K250126

FDA listed device types

Electrosurgical, Cutting & Coagulation & Accessories 1Laparoscope, General & Plastic Surgery 1Instrument, Manual, Surgical, General Use 1Applier, Surgical, Clip 1

Registration details (sample)

Market	Identifier	Name	Class / date
EU	08800042706142	ArtiSential Clip Applier	Class IIa
EU	08800042706128	ArtiSential Clip Applier	Class IIa
EU	08800042706135	ArtiSential Clip Applier	Class IIa
EU	08800042706111	ArtiSential Clip Applier	Class IIa
UK	11490	ArtiSeal Vessel Sealing System - ArtiSeal Generator	Class IIb
UK	61872	ArtiSential Laparoscopic Instruments-Electrodes	Class IIb
UK	61875	ArtiSential Laparoscopic Instruments-Electrodes	Class IIb
US	K250126	ArtiSeal Vessel Sealing System - ArtiSeal Instruments (AS01M)	2025-10-21
US	K241138	ArtiSeal Vessel Sealing System-ArtiSeal Instruments; ArtiSeal Vessel Sealing System-ArtiSeal Generator	2024-11-15
US	K240657	ArtiSential Laparoscopic Instruments-Electrodes (AMHD01-LH); ArtiSential Laparoscopic Instruments-Electrodes (AMHD01S-LH); ArtiSential Laparoscopic Instruments-Electrodes (AMHD01L-LH); ArtiSential Laparoscopic Instruments-Electrodes (5AMHD01-LH); ArtiSential Laparoscopic Instruments-Electrodes (5AMHD01S-LH); ArtiSential Laparoscopic Instruments-Electrodes (AMHD01-FH); ArtiSential Laparoscopic Instruments-Electrodes (AMHD01S-FH); ArtiSential Laparoscopic Instruments-Electrodes (AMHD01L-	2024-06-06