Home / Companies / Livsmed, Inc.

Livsmed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250126ArtiSeal Vessel Sealing System - ArtiSeal Instruments (AS01M)October 21, 2025
K241138ArtiSeal Vessel Sealing System-ArtiSeal Instruments; ArtiSeal Vessel Sealing System-ArtiSeal GeneratNovember 15, 2024
K240657ArtiSential Laparoscopic Instruments-Electrodes (AMHD01-LH); ArtiSential Laparoscopic Instruments-ElJune 6, 2024
K230498ArtiSential Laparoscopic Instruments-ElectrodesJune 5, 2023
K230539ArtiSential Laparoscopic Instruments-ElectrodesApril 27, 2023
K230499ArtiSential Laparoscopic Instruments-ElectrodesApril 26, 2023
K220384ArtiSential Laparoscopic Instruments-ElectrodesFebruary 24, 2022
K212500ArtiSential TrocarDecember 3, 2021
K203580ArtiSential Laparoscopic Instruments-ElectrodesApril 30, 2021
K200875ArtiSential Laparoscopic Instruments - ElectrodesJune 17, 2020
K200501ArtiSential Laparoscopic Instrument-ElectrodesMay 11, 2020
K190909ArtiSential Bipolar Fenestrated ForcepsFebruary 13, 2020