FDA applicant

Avanca Medical Devices, Inc.

Albuquerque, NM3 decisions2005–20050 recalls

FDA records 3 decisions for Avanca Medical Devices, Inc. (Albuquerque, NM) in 2005: 3 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and MEG (Syringe, Antistick). Its devices cite 4 predicates, 1 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Avanca Medical Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Avanca Medical Devices, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?