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

NOMAD Pro 3

K Number: K253864 · Decision Mar 20, 2026
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
189
Applicant Total
2
Review Days
107

Basic Information

Device Name
NOMAD Pro 3
K Number
K253864
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dental Imaging Technologies Corporation
Date Received
December 3, 2025
Decision Date
March 20, 2026
Product Code
EHD
Advisory Committee
Dental
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
EHD Unit, X-Ray, Extraoral With Timer

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K Number Device Name
K233053 DEXIS Ti2 Intraoral Sensor, DEXIS IXS Size 1 Intraoral Sensor, DEXIS IXS Size 2 Intraoral Sensor