Applied Medical Resources Corporation - FDA 510(k) Cleared Devices
Recent clearances: Alexis lighted wound protector-retractor, flexible, extra small (cl312), Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402), Voyant® Electrosurgical Generator (EA030/Electrosurgical Generator)
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Applied Medical Resources Corporation General & Plastic Surgery ✕
9 devices
Cleared
Apr 24, 2026
Alexis lighted wound protector-retractor, flexible, extra small (cl312)
General & Plastic Surgery
30d
Cleared
Feb 23, 2026
Alexis® Lighted Wound Protector-Retractor, Rigid, Medium (CL402)
General & Plastic Surgery
102d
Cleared
Oct 31, 2025
Voyant® Electrosurgical Generator (EA030/Electrosurgical Generator)
General & Plastic Surgery
91d
Cleared
Nov 01, 2023
Inzii Ripstop Redeployable Retrieval System
General & Plastic Surgery
44d
Cleared
Oct 14, 2022
Voyant Maryland Fusion device with Single-Step Activation (EB212, EB213, EB214)
General & Plastic Surgery
74d
Cleared
Nov 22, 2019
Applied Medical Laparoscopic Linear Cutter
General & Plastic Surgery
281d
Cleared
Apr 13, 2018
Voyant Open Fusion Device
General & Plastic Surgery
28d
Cleared
Feb 13, 2018
Voyant 5mm Fusion Device
General & Plastic Surgery
165d
Cleared
Aug 07, 2017
Epix Electrosurgical Probe with Smoke Evacuation
General & Plastic Surgery
61d