GENIOVA aligners— 510(k) K233152

Name: FDA 510(k) clearance K233152
Creator: U.S. Food and Drug Administration
Published: 2024-12-12

Substantially Equivalent

Geniova Technologies Sociedad Limitada

FDA 510(k) clearance K233152 for GENIOVA aligners, Substantially Equivalent on 2024-12-12. Applicant: Geniova Technologies Sociedad Limitada. Device class: 2.

Clearance details

Applicant: Geniova Technologies Sociedad Limitada
Product code: Code NXC
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 2023-09-27
Decision date: 2024-12-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madrid, ES

Download summary PDF View on FDA.gov ↗

Recent devices under product code NXC

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K260527 — FACE4D Aligner2026-07-02
K260788 — Smylio Aligners2026-05-08
K260722 — SureSmile Aligner (ASSY500020)2026-04-15
K253282 — ZSmile System2026-02-03
K251454 — Clear Aligner (SCF-3348)2026-01-07

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.