Applied Medical Resources Corp. - FDA 510(k) Cleared Devices
45
Total
45
Cleared
0
Denied
Applied Medical Resources Corp. has 45 FDA 510(k) cleared medical devices. Based in Rancho Santa, US.
Latest FDA clearance: Nov 2025. Active since 2001. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Applied Medical Resources Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Applied Medical Resources Corp.
45 devices
Cleared
Nov 04, 2025
Voyant® Open Fusion Device (EB240/Open Fusion)
General & Plastic Surgery
68d
Cleared
Oct 31, 2025
Kii Structural Balloon Access System
General & Plastic Surgery
88d
Cleared
Oct 02, 2025
GelPOINT V-Path Transvaginal Access Platform with Retroperitoneal Access Device
Obstetrics & Gynecology
367d
Cleared
Jun 05, 2020
Voyant Open Fusion Device
General & Plastic Surgery
31d
Cleared
Apr 08, 2020
Voyant Maryland Fusion Device
General & Plastic Surgery
30d
Cleared
Dec 20, 2019
Voyant 5mm Fusion Device, Voyant Maryland Fusion Device
General & Plastic Surgery
23d
Cleared
Sep 06, 2019
Transvaginal Access Platform
Obstetrics & Gynecology
115d
Cleared
Nov 14, 2018
Voyant Maryland Fusion Device
General & Plastic Surgery
50d
Cleared
Oct 11, 2018
Voyant Electrosurgical Generator
General & Plastic Surgery
52d
Cleared
Aug 30, 2018
Dissecting Balloon System
General & Plastic Surgery
31d
Cleared
Jul 20, 2017
GelPOINT Path Transanal Access Platform
Gastroenterology & Urology
42d
Cleared
Jan 24, 2014
EPIX ELECTROSURGICAL PROBE SPATULA TIP, EPIX ELECTROSURGICAL PROBE L-HOOK...
General & Plastic Surgery
184d
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