FDA applicant

David Ayres Medical Co.

Reno, NV1 decision1990–19900 recalls

FDA records 1 decision for David Ayres Medical Co. (Reno, NV) in 1990: 1 510(k) clearance. All are in product code LDQ (Unnamed device). 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, general hospital panel, where it files most

How often FDA has decided David Ayres Medical Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for David Ayres Medical Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like David Ayres Medical Co.’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

Other applicant names beginning “David”

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

David A. Fuccillo, Ph.D. 9 David Simmonds Co., Inc. 3 David Bull Laboratories, USA, Inc. 2 David Craig Marketing, Inc. 1 David C. Bishop, Ph.D. 1 David F. Trungale 1 David Hendricks, C.P.O. 1 David J. Slutsky MD 1 David Cott Co. 1 David Clark Company, Inc. 1 David Medical Products Co.,Ltd 1 David Connell 1

David Ayres Medical Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “David”