Last synced on 2 May 2025 at 11:05 pm

Denture Base

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243103
510(k) Type
Traditional
Applicant
Riton 3D Technology Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/23/2024
Days to Decision
84 days
Submission Type
Summary

Denture Base

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243103
510(k) Type
Traditional
Applicant
Riton 3D Technology Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/23/2024
Days to Decision
84 days
Submission Type
Summary