FDA applicant

Clay Kennard

Oklahoma City, OK1 decision2006–20060 recalls

FDA records 1 decision for Clay Kennard (Oklahoma City, OK) in 2006: 1 510(k) clearance. All are in product code GBM (Catheter, Urethral). Its devices cite 1 predicate, 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, gastroenterology and urology panel, where it files most

How often FDA has decided Clay Kennard’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clay Kennard since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Clay Kennard’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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Other applicant names beginning “Clay”

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

Clay-Park Labs, Inc. 1 Clay Adams, Div. Becton Dickinson & Co. 1

Clay Kennard

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Clay”