FDA applicant

Adven Medical

Lubbock, TX6 decisions1994–20020 recalls

FDA records 6 decisions for Adven Medical (Lubbock, TX) from 1994 to 2002: 6 510(k) clearances. Most are in product codes HWE (Instrument, Surgical, Orthopedic, Ac-Powered…) and JOW (Sleeve, Limb, Compressible). Its devices cite 2 predicates, 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Adven Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Adven Medical

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?