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

DS Core CBCT Anatomy

K Number: K260785 · Decision Apr 23, 2026
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
303
Applicant Total
65
Review Days
44

Basic Information

Device Name
DS Core CBCT Anatomy
K Number
K260785
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Sirona
Date Received
March 10, 2026
Decision Date
April 23, 2026
Product Code
QIH
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
QIH Automated Radiological Image Processing Software

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