FDA applicant

Habley Medical Technology Corp.

Laguana Hills, CA5 decisions1987–19960 recalls

FDA records 5 decisions for Habley Medical Technology Corp. (Laguana Hills, CA) from 1987 to 1996: 5 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and JKA (Tubes, Vials, Systems, Serum Separators, Blood…). Its devices cite 1 predicate, 0 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 Habley Medical Technology Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Habley Medical Technology Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Habley Medical Technology Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?