FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

A.B. DENTAL DEVICES Dental Implants System

K Number: K162482 · Decision Sep 15, 2017
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
4
Review Days
374

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Basic Information

Device Name
A.B. DENTAL DEVICES Dental Implants System
K Number
K162482
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 Device , Ltd.
Date Received
September 6, 2016
Decision Date
September 15, 2017
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

Other 510(k) clearances with the same product code (DZE), ordered by most recent decision date.

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

K Number Device Name
K202144 A.B. Dental Devices Dental Implants System
K182455 A.B. DENTAL DEVICES Dental Implants System
K181381 A.B. Dental Devices Dental Implants System