MODIFICATION TO ORTHODONTIC COMPOSITE BRACKET SYSTEM— 510(k) K050730

Name: FDA 510(k) clearance K050730
Creator: U.S. Food and Drug Administration
Published: 2005-03-31

Substantially Equivalent

Ultradent Products, Inc.

FDA 510(k) clearance K050730 for MODIFICATION TO ORTHODONTIC COMPOSITE BRACKET SYSTEM, Substantially Equivalent on 2005-03-31. Applicant: Ultradent Products, Inc.. Device class: 2.

Clearance details

Applicant: Ultradent Products, Inc.
Product code: Code DYW
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 2005-03-21
Decision date: 2005-03-31
Decision: Substantially Equivalent
Clearance type: Special
Location: South Jordan, UT, US

Download summary PDF View on FDA.gov ↗

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