FDA applicant

Acd Medical Innovation Corp.

Littleton, CO1 decision2007–20070 recalls

FDA records 1 decision for Acd Medical Innovation Corp. (Littleton, CO) in 2007: 1 510(k) clearance. All are in product code FCG (Biopsy Needle). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Acd Medical Innovation Corp.

Which product codes does it file in?

What has FDA decided for it lately?