FDA applicant

Laclede, Inc.

Rancho Dominguez, CA5 decisions2006–20240 recalls

FDA records 5 decisions for Laclede, Inc. (Rancho Dominguez, CA) from 2006 to 2024: 5 510(k) clearances. Most are in product codes LFD (Saliva, Artificial) and NUC (Lubricant, Personal). Its devices cite 12 predicates, 3 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 Laclede, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2007high 1 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Laclede, 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?