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

DS Core Detect

K Number: K253009 · Decision Jan 7, 2026
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
36
Applicant Total
21
Review Days
110

Basic Information

Device Name
DS Core Detect
K Number
K253009
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2070
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentsply Sirona, Inc.
Date Received
September 19, 2025
Decision Date
January 7, 2026
Product Code
MYN
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
MYN Analyzer, Medical Image

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