510(k) Report

FDA applicant

Alpha-Omega Services, Inc.

Bellflower, CA9 decisions1997–20240 recalls

FDA records 9 decisions for Alpha-Omega Services, Inc. (Bellflower, CA) from 1997 to 2024: 9 510(k) clearances. Most are in product codes JAQ (System, Applicator, Radionuclide…) and KXK (Source, Brachytherapy, Radionuclide). Its devices cite 7 predicates, 3 of them its own earlier devices. 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, radiology panel, where it files most

How often FDA has decided Alpha-Omega Services, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2024

2007: 42011: 12024: 2
2007high 4 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Alpha-Omega Services, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Alpha-Omega Services, 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 “Alpha-Omega”

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