NUBRACE INVISIBLE REMOVABLE ORTHODONTICS— 510(k) K073121

Name: FDA 510(k) clearance K073121
Creator: U.S. Food and Drug Administration
Published: 2009-02-12

Substantially Equivalent

Nubrace, Inc.

FDA 510(k) clearance K073121 for NUBRACE INVISIBLE REMOVABLE ORTHODONTICS, Substantially Equivalent on 2009-02-12. Applicant: Nubrace, Inc.. Device class: 2.

Clearance details

Applicant: Nubrace, Inc.
Product code: Code NXC
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 2007-11-05
Decision date: 2009-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code NXC

product code NXC

Injury: 15,206
Malfunction: 2,576
Other: 9
Total: 17,791

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.