FDA applicant

Apimeds, Inc.

Greenwood Village, CO1 decision2009–20090 recalls

FDA records 1 decision for Apimeds, Inc. (Greenwood Village, CO) in 2009: 1 510(k) clearance. All are in product code HIR (Perineometer). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

1in 2009

2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Apimeds, Inc. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Apimeds, Inc.

Which product codes does it file in?

What has FDA decided for it lately?