FDA applicant

Gary D. Keller

Sherman, TX1 decision1985–19850 recalls

FDA records 1 decision for Gary D. Keller (Sherman, TX) in 1985: 1 510(k) clearance. All are in product code IWY (Holder, Head, Radiographic). 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 Gary D. Keller’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Gary D. Keller since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Gary”

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

Gary E. Hall, Dds 2 Gary A. Gelbfish 1 Gary Plastic Packaging Corp. 1 Gary Giancarlo 1

Gary D. Keller

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Gary”