Livsmed, Inc.
Livsmed, Inc. appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Oct 21, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K250126 | ArtiSeal Vessel Sealing System - ArtiSeal Instruments (AS01M) | Oct 21, 2025 |
| K241138 | ArtiSeal Vessel Sealing System-ArtiSeal Instruments; ArtiSeal Vessel Sealing System-ArtiSeal Generat | Nov 15, 2024 |
| K240657 | ArtiSential Laparoscopic Instruments-Electrodes (AMHD01-LH); ArtiSential Laparoscopic Instruments-El | Jun 6, 2024 |
| K230498 | ArtiSential Laparoscopic Instruments-Electrodes | Jun 5, 2023 |
| K230539 | ArtiSential Laparoscopic Instruments-Electrodes | Apr 27, 2023 |
| K230499 | ArtiSential Laparoscopic Instruments-Electrodes | Apr 26, 2023 |
| K220384 | ArtiSential Laparoscopic Instruments-Electrodes | Feb 24, 2022 |
| K212500 | ArtiSential Trocar | Dec 3, 2021 |
| K203580 | ArtiSential Laparoscopic Instruments-Electrodes | Apr 30, 2021 |
| K200875 | ArtiSential Laparoscopic Instruments - Electrodes | Jun 17, 2020 |
| K200501 | ArtiSential Laparoscopic Instrument-Electrodes | May 11, 2020 |
| K190909 | ArtiSential Bipolar Fenestrated Forceps | Feb 13, 2020 |