FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Dental X-Ray Device (Ai Ray Lite, Ai Ray Pro, Master Ray )

K Number: K251438 · Decision Sep 4, 2025
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
189
Applicant Total
14
Review Days
118

Basic Information

Device Name
Dental X-Ray Device (Ai Ray Lite, Ai Ray Pro, Master Ray )
K Number
K251438
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.1800
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Guilin Woodpecker Medical Instrument Co., Ltd.
Date Received
May 9, 2025
Decision Date
September 4, 2025
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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