510(k) Report

FDA applicant

Davis Lead Aprons, Inc.

Houston, TX3 decisions1992–19920 recalls

FDA records 3 decisions for Davis Lead Aprons, Inc. (Houston, TX) in 1992: 3 510(k) clearances. All are in product code KPY (Shield, Protective, Personnel). 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, radiology panel, where it files most

How often FDA has decided Davis Lead Aprons, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Davis Lead Aprons, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • KPYShield, Protective, Personnel3decisions

What has FDA decided for it lately?

  • K912378Davis Lead Apron/Radiographic Various Cat. NumbersDavis Lead Aprons, Inc. · 1992
  • K912327Davis Lead Apron Gonadal Shield-Various Cat. Nos.Davis Lead Aprons, Inc. · 1992
  • K912326Davis Lead Apron - Various Catalogue NumbersDavis Lead Aprons, Inc. · 1992

All 3 as Davis Lead Aprons, Inc. →

Other applicant names beginning “Davis”

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

Davis & Geck, Inc. 46Davis Schottlander & Davis, Ltd. 7Davis Assoc. 1Davis Medical 1Davis-Smith Corp. 1Davis Positioning Systems, Inc. 1