FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Primevision 3D

K Number: K253959 · Decision Feb 5, 2026
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
65
Review Days
57

Basic Information

Device Name
Primevision 3D
K Number
K253959
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Sirona
Date Received
December 10, 2025
Decision Date
February 5, 2026
Product Code
OAS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OAS X-Ray, Tomography, Computed, Dental

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