Applied Medical Resources Corporation
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 11
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K253531 | Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402); Alexis® Lighted Wound Protector-Re | February 23, 2026 |
| K252412 | Voyant® Electrosurgical Generator (EA030/Electrosurgical Generator) | October 31, 2025 |
| K232880 | Inzii Ripstop Redeployable Retrieval System | November 1, 2023 |
| K222284 | Voyant Maryland Fusion device with Single-Step Activation (EB212, EB213, EB214) | October 14, 2022 |
| K220969 | GelPOINT V-Path Vaginal Access System | September 16, 2022 |
| K211043 | Alexis Contained Extraction System | March 31, 2022 |
| K202049 | Python Catheter/Over-the-Wire Latis Graft Cleaning Catheter | September 7, 2021 |
| K190331 | Applied Medical Laparoscopic Linear Cutter | November 22, 2019 |
| K180699 | Voyant Open Fusion Device | April 13, 2018 |
| K172624 | Voyant 5mm Fusion Device | February 13, 2018 |
| K171684 | Epix Electrosurgical Probe with Smoke Evacuation | August 7, 2017 |