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.
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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