FDA applicant

Lil Drug Store Products, Inc.

Cedar Rapids, IA3 decisions2008–20100 recalls

FDA records 3 decisions for Lil Drug Store Products, Inc. (Cedar Rapids, IA) from 2008 to 2010: 3 510(k) clearances. Most are in product codes NUC (Lubricant, Personal) and LKX (Device, Thermal, Hemorrhoids). Its devices cite 3 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Lil Drug Store Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2010

2008high 2 (2010) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Lil Drug Store Products, Inc. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Lil Drug Store Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Lil Drug Store Products, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?