FDA applicant

Lh Medical Products, Inc.

San Dimas, CA3 decisions2001–20010 recalls

FDA records 3 decisions for Lh Medical Products, Inc. (San Dimas, CA) in 2001: 3 510(k) clearances. All are in product code KNT (Tubes, Gastrointestinal (And Accessories)). 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 Lh Medical Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lh Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Lh Medical Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?