FDA applicant

Allan Walling Medical Equipment Co.

Dallas, TX1 decision1994–19940 recalls

FDA records 1 decision for Allan Walling Medical Equipment Co. (Dallas, TX) in 1994: 1 510(k) clearance. All are in product code LKY (Device, External Penile Rigidity). 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 Allan Walling Medical Equipment Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Allan Walling Medical Equipment Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Allan”

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

Allan V. Marse 1 Allan Rehnstrom AB 1 Allan Schulman,D.D.S., M.S. 1

Allan Walling Medical Equipment Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Allan”