Last synced on 14 November 2025 at 11:06 pm

Lumos 3DX

Page Type
Cleared 510(K)
510(k) Number
K223780
510(k) Type
Traditional
Applicant
3Dio
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2023
Days to Decision
202 days
Submission Type
Summary

Lumos 3DX

Page Type
Cleared 510(K)
510(k) Number
K223780
510(k) Type
Traditional
Applicant
3Dio
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2023
Days to Decision
202 days
Submission Type
Summary