510(k) Report

FDA applicant

Westridge Laboratories, Inc.

Santa Ana, CA3 decisions2006–20240 recalls

FDA records 3 decisions for Westridge Laboratories, Inc. (Santa Ana, CA) from 2006 to 2024: 3 510(k) clearances. All are in product code NUC (Lubricant, Personal). Its devices cite 4 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 Westridge Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2015: 12024: 1
2007high 1 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Westridge Laboratories, 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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Which product codes does it file in?

  • NUCLubricant, Personal3decisions

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K051295I-D GlideWestridge Laboratories, Inc. · 20062cite it
  • K240745ID Free Personal LubricantWestridge Laboratories, Inc. · 20241cites it

What has FDA decided for it lately?

  • K240745ID Free Personal LubricantWestridge Laboratories, Inc. · 2024
  • K141767ID Millennium, ID Moments SiliconeWestridge Laboratories, Inc. · 2015
  • K051295I-D GlideWestridge Laboratories, Inc. · 2006

All 3 as Westridge Laboratories, Inc. →