FDA.reportPublic FDA data

LivsMed Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30148487203014848720LivsMed Inc.1N2027-01-01201, 202, 203, 204, 204-1, 208, 304, 406, 602-1, 603, D-dong 108, 302, 402-1, 504, 506-1, 603, 706, 708, E-do Seongnam-si Gyeonggi KR 13516

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2215791984429193K250126ArtiSeal Vessel Sealing System - ArtiSeal Instruments (AS01M)GEI2025-10-21
2215791691104338K241138ArtiSeal Vessel Sealing System-ArtiSeal Instruments; ArtiSeal Vessel Sealing System-ArtiSeal GeneratorGEI2024-11-15
2215791763356429K240657ArtiSential 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-GEI2024-06-06
2215791027433469K230539ArtiSential Laparoscopic Instruments-ElectrodesGEI2023-04-27
2215791796764753K230499ArtiSential Laparoscopic Instruments-ElectrodesGEI2023-04-26
2215791146277045K230498ArtiSential Laparoscopic Instruments-ElectrodesGEI2023-06-05
2215791041515254K212500ArtiSential TrocarGCJ2021-12-03
2215791772000707K190909ArtiSential Bipolar Fenestrated ForcepsGEI2020-02-13
2215791434529863
2215791560567918

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEI72025-10-21
GCJ12021-12-03

PMN#