Denture Base Resin (PN-Denture (Red, White))— 510(k) K241673

Name: FDA 510(k) clearance K241673
Creator: U.S. Food and Drug Administration
Published: 2024-10-15

Substantially Equivalent

Shenzhen Piocreat 3D Technology Co., Ltd.

FDA 510(k) clearance K241673 for Denture Base Resin (PN-Denture (Red, White)), Substantially Equivalent on 2024-10-15. Applicant: Shenzhen Piocreat 3D Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Piocreat 3D Technology Co., Ltd.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2024-06-11
Decision date: 2024-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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