ANTHOGYR CONTRA ANGLES AND HANDPIECES— 510(k) K060317

Name: FDA 510(k) clearance K060317
Creator: U.S. Food and Drug Administration
Published: 2006-04-28

Substantially Equivalent

Est. Anthogyr

FDA 510(k) clearance K060317 for ANTHOGYR CONTRA ANGLES AND HANDPIECES, Substantially Equivalent on 2006-04-28. Applicant: Est. Anthogyr. Device class: 1.

Clearance details

Applicant: Est. Anthogyr
Product code: Code EGS
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 2006-02-08
Decision date: 2006-04-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sallanches, FR

Download summary PDF View on FDA.gov ↗

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K240183 — Star E900 Handpiece Series2024-09-19
K230106 — General Cutting Straight2023-05-24
K222518 — FX Contra2022-11-17

More clearances from Est. Anthogyr

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K070084 — MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROL2007-03-08
K020431 — FIBIOCORE2002-07-03

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.