Skip to the page

Data / Medical devices / South Korea / LivsMed Inc.

LivsMed Inc.: FDA-registered device maker in Seongnam-si Gyeonggi, South Korea, 7 510(k) clearances

LivsMed Inc. is registered with the FDA (registration 3014848720) in Seongnam-si Gyeonggi, South Korea. It lists 4 device types. The FDA files 7 510(k) clearances under its listings, the newest dated October 21, 2025. Registered through 2027. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3014848720
Address
201, 202, 203, 204, 204-1, 208, 304, 406, 602-1, 603, D-dong 108, 302, 402-1, 504, 506-1, 603, 706, 708, E-dong, Seongnam-si Gyeonggi, South Korea, 13516
Owner or operator
LivsMed (10058340)
Roles
Manufacturer
First device listed
August 28, 2018
Registered through
2027
Brand names listed
ArtiSeal Vessel Sealing System - ArtiSeal Generator, ArtiSeal Vessel Sealing System - ArtiSeal Instruments, ArtiSential Bipolar Blunt tip Dissector, ArtiSential Bipolar Fenestrated Forceps, ArtiSential Bipolar Maryland Dissector, ArtiSential Bipolar Precise Dissector, ArtiSential Clinch Forceps, ArtiSential Clip Applier Large and more

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
October 21, 2025K250126ArtiSeal Vessel Sealing System - ArtiSeal Instruments (AS01M)GEISubstantially EquivalentLivsmed, Inc.accessdata.fda.gov
November 15, 2024K241138ArtiSeal Vessel Sealing System-ArtiSeal Instruments; ArtiSeal Vessel Sealing System-ArtiSeal GeneratorGEISubstantially EquivalentLivsmed, Inc.accessdata.fda.gov
June 6, 2024K240657ArtiSential 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-GEISubstantially EquivalentLivsmed, Inc.accessdata.fda.gov
June 5, 2023K230498ArtiSential Laparoscopic Instruments-ElectrodesGEISubstantially EquivalentLivsmed, Inc.accessdata.fda.gov
April 27, 2023K230539ArtiSential Laparoscopic Instruments-ElectrodesGEISubstantially EquivalentLivsmed, Inc.accessdata.fda.gov
April 26, 2023K230499ArtiSential Laparoscopic Instruments-ElectrodesGEISubstantially EquivalentLivsmed, Inc.accessdata.fda.gov
December 3, 2021K212500ArtiSential TrocarGCJSubstantially EquivalentLivsmed, Inc.accessdata.fda.gov

Compare with other makers

Updated October 21, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.