FDA applicant

Aso Corp.

Sarasota, FL4 decisions1993–20090 recalls

FDA records 4 decisions for Aso Corp. (Sarasota, FL) from 1993 to 2009: 4 510(k) clearances. Most are in product codes KGX (Tape And Bandage, Adhesive) and EFQ (Gauze/Sponge, Internal). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Aso, LLC”.

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 Aso Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Aso Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?