Denture Base— 510(k) K243103

Name: FDA 510(k) clearance K243103
Creator: U.S. Food and Drug Administration
Published: 2024-12-23

Substantially Equivalent

Riton 3D Technology Co., Ltd.

FDA 510(k) clearance K243103 for Denture Base, Substantially Equivalent on 2024-12-23. Applicant: Riton 3D Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Riton 3D Technology Co., Ltd.
Product code: Code EBI
Device class: Class 2
Regulation: 21 CFR 872.3760
Advisory panel: Dental
Date received: 2024-09-30
Decision date: 2024-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guangzhou, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code EBI

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K261802 — Glidewell Denture Base Resin2026-08-27
K261626 — UltraPrint Flexible Denture UV2026-08-13
K262681 — NanoCeram Resin2026-07-31
K262300 — Denture Base Resin V22026-07-08
K261474 — DENTCA Tru Flexible2026-07-01

Adverse events under product code EBI

product code EBI

Other: 1
Total: 1

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.