Applied Medical Resources Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Applied Medical Resources Corp. - FDA 510(k) Cleared Devices
Recent clearances: Voyant® Open Fusion Device (EB240/Open Fusion), Kii Structural Balloon Access System, GelPOINT V-Path Transvaginal Access Platform with Retroperitoneal Access Device
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.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Applied Medical Resources Corp.
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