510(k) Report

FDA applicant

Alliance Medical Technologies, Inc.

Irvine,1 decision1997–19970 recalls

FDA records 1 decision for Alliance Medical Technologies, Inc. (Irvine,) in 1997: 1 original PMA approval. All are in product code LWQ (Heart-Valve, Mechanical). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Alliance Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alliance Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Alliance Medical Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Alliance Medical Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Alliance”

FDA records each applicant name separately; these may or may not be the same firm.