Spark Clear Aligner System— 510(k) K203737

Substantially Equivalent

Ormco Corporation

FDA 510(k) clearance K203737 for Spark Clear Aligner System, Substantially Equivalent on 2021-03-22. Applicant: Ormco Corporation.

Clearance details

Applicant: Ormco Corporation
Product code: Code NXC
Advisory panel: Dental
Date received: 2020-12-22
Decision date: 2021-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Brea, CA, US

Download summary PDF View on FDA.gov ↗

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.