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

A.B. DENTAL DEVICES DENTAL IMPLANTS SYSTEM

K Number: K132125 · Decision Jan 21, 2014
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
4
Review Days
195

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Basic Information

Device Name
A.B. DENTAL DEVICES DENTAL IMPLANTS SYSTEM
K Number
K132125
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
A.B. Dental Devices , Ltd.
Date Received
July 10, 2013
Decision Date
January 21, 2014
Product Code
DZE
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DZE Implant, Endosseous, Root-Form

Similar 510(k) Clearances

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Other Clearances by A.B. Dental Devices , Ltd.

K Number Device Name
K250806 Dental Implant System
K112440 AB DENTAL DEVICES IMPLANTS AND ACCESSORIES
K051719 A.B. DENTAL DEVICES