Medical Device Manufacturer · KR , Seongnam-Si

Livsmed, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 2020

Recent clearances: ArtiSeal Vessel Sealing System - ArtiSeal Instruments (AS01M), ArtiSeal Vessel Sealing System-ArtiSeal Instruments, ArtiSential Laparoscopic Instruments-Electrodes (AMHD01-LH)

12
Total
12
Cleared
0
Denied

FDA 510(k) Regulatory Record - Livsmed, Inc. General & Plastic Surgery ✕

12 devices
1-12 of 12
Cleared Oct 21, 2025
ArtiSeal Vessel Sealing System - ArtiSeal Instruments (AS01M)
K250126 · GEI
General & Plastic Surgery · 277d
Cleared Nov 15, 2024
ArtiSeal Vessel Sealing System-ArtiSeal Instruments
K241138 · GEI
General & Plastic Surgery · 205d
Cleared Jun 06, 2024
ArtiSential Laparoscopic Instruments-Electrodes (AMHD01-LH)
K240657 · GEI
General & Plastic Surgery · 90d
Cleared Jun 05, 2023
ArtiSential Laparoscopic Instruments-Electrodes
K230498 · GEI
General & Plastic Surgery · 101d
Cleared Apr 27, 2023
ArtiSential Laparoscopic Instruments-Electrodes
K230539 · GEI
General & Plastic Surgery · 59d
Cleared Apr 26, 2023
ArtiSential Laparoscopic Instruments-Electrodes
K230499 · GEI
General & Plastic Surgery · 61d
Cleared Feb 24, 2022
ArtiSential Laparoscopic Instruments-Electrodes
K220384 · GEI
General & Plastic Surgery · 14d
Cleared Dec 03, 2021
ArtiSential Trocar
K212500 · GCJ
General & Plastic Surgery · 116d
Cleared Apr 30, 2021
ArtiSential Laparoscopic Instruments-Electrodes
K203580 · GEI
General & Plastic Surgery · 144d
Cleared Jun 17, 2020
ArtiSential Laparoscopic Instruments - Electrodes
K200875 · GEI
General & Plastic Surgery · 77d
Cleared May 11, 2020
ArtiSential Laparoscopic Instrument-Electrodes
K200501 · GEI
General & Plastic Surgery · 73d
Cleared Feb 13, 2020
ArtiSential Bipolar Fenestrated Forceps
K190909 · GEI
General & Plastic Surgery · 311d
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