FDA applicant

Asc Corp.

Troy, MI1 decision1986–19860 recalls

FDA records 1 decision for Asc Corp. (Troy, MI) in 1986: 1 510(k) clearance. All are in product code LBE (Stroller, Adaptive). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Asc Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Asc Corp.

Which product codes does it file in?

What has FDA decided for it lately?