510(k) Report

FDA applicant

Whitmore Ent., Inc.

San Antonio, TX2 decisions1993–19930 recalls

FDA records 2 decisions for Whitmore Ent., Inc. (San Antonio, TX) in 1993: 2 510(k) clearances. Most are in product codes KPR (System, X-Ray, Stationary) and FWZ (Operating Room Accessories Table Tray). 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 Whitmore Ent., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Whitmore Ent., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Whitmore Ent., 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?

  • KPRSystem, X-Ray, Stationary1decision
  • FWZOperating Room Accessories Table Tray1decision

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.

  • K933778Whitmore Ankle X-Ray Extension (Axe)Whitmore Ent., Inc. · 19931cites it

What has FDA decided for it lately?

  • K933778Whitmore Ankle X-Ray Extension (Axe)Whitmore Ent., Inc. · 1993
  • K931037Whitmore Vacuum-Lock Spinal Frame (VLSF-100)Whitmore Ent., Inc. · 1993

All 2 as Whitmore Ent., Inc. →