ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE— 510(k) K023953

Name: FDA 510(k) clearance K023953
Creator: U.S. Food and Drug Administration
Published: 2003-02-14

Substantially Equivalent

St. George Technology, Inc.

FDA 510(k) clearance K023953 for ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE, Substantially Equivalent on 2003-02-14. Applicant: St. George Technology, Inc.. Device class: 1.

Clearance details

Applicant: St. George Technology, Inc.
Product code: Code EGS
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 2002-11-27
Decision date: 2003-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, NC, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code EGS

product code EGS

Injury: 356
Malfunction: 759
Total: 1,115

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.