FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

DENTRIa series

K Number: K160140 · Decision Sep 30, 2016
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
9
Review Days
253

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Basic Information

Device Name
DENTRIa series
K Number
K160140
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hdx Will Corp.
Date Received
January 21, 2016
Decision Date
September 30, 2016
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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Other Clearances by Hdx Will Corp.

K Number Device Name
K211159 eco-x Series (eco-x, eco-x-s)
K211114 Will3D
K212254 DENTRIa series (DENTRIa, DENTRI-Ca, DENTRI-Sa)
K192700 Xcam
K190357 Star-X, Intraoral X-ray System
K181297 DENTIOIII series (DENTIOIII, DENTIOIII-S)
K172168 WillCeph
K170180 Will3D