FDA applicant

St. George Technology, Inc.

York, PA4 decisions1994–20030 recalls

FDA records 4 decisions for St. George Technology, Inc. (York, PA) from 1994 to 2003: 4 510(k) clearances. Most are in product codes EBI (Resin, Denture, Relining, Repairing, Rebasing) and EGS (Handpiece, Contra- And Right-Angle Attachment…). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 St. George Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for St. George Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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St. George Technology, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?