510(k) Report

FDA applicant

Clay-Park Labs, Inc.

Washington, DC1 decision2001–20010 recalls

FDA records 1 decision for Clay-Park Labs, Inc. (Washington, DC) in 2001: 1 510(k) clearance. All are in product code NUC (Lubricant, Personal). 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 Clay-Park Labs, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clay-Park Labs, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Clay-Park Labs, 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

Which product codes does it file in?

  • NUCLubricant, Personal1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K012203Clay-Park Labs, Inc. - Lubricating JellyClay-Park Labs, Inc. · 20011cites it

What has FDA decided for it lately?

  • K012203Clay-Park Labs, Inc. - Lubricating JellyClay-Park Labs, Inc. · 2001

The one decision as Clay-Park Labs, Inc. →

Other applicant names beginning “Clay-Park”

FDA records each applicant name separately; these may or may not be the same firm.

Clay Kennard 1Clay Adams, Div. Becton Dickinson & Co. 1