FDA applicant

Gary E. Hall, Dds

Unnamed device, MI2 decisions1984–19870 recalls

FDA records 2 decisions for Gary E. Hall, Dds (Unnamed device, MI) from 1984 to 1987: 2 510(k) clearances. Most are in product codes EAH (Cone, Radiographic, Lead-Lined) and 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, dental panel, where it files most

How often FDA has decided Gary E. Hall, Dds’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Gary E. Hall, Dds since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Gary E. Hall, Dds 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 A. Gelbfish 1 Gary Plastic Packaging Corp. 1 Gary D. Keller 1 Gary Giancarlo 1

Gary E. Hall, Dds

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Gary”