FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

Dental Implant OKTAGON Bone Level

K Number: K143539 · Decision Aug 31, 2015
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
14
Review Days
259

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Basic Information

Device Name
Dental Implant OKTAGON Bone Level
K Number
K143539
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hager& Meisinger GmbH
Date Received
December 15, 2014
Decision Date
August 31, 2015
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

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Other Clearances by Hager& Meisinger GmbH

K Number Device Name
K250123 Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)
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K201210 The Micro Screw System, Micro Screw System Basic
K173819 MyPlant II Implant System
K180360 OKTAGON Implant System
K170287 Dental Implants OKTAGON Bone Level Tapered Design
K162073 Dental Implants OKTAGON Tissue Level and Bone Level
K160132 Dental Implant Abutment OKTAGON Bone Level RC, Dental Implant Abutment OKTAGON Bone Level NC
K132214 ABUTMENT RP, ABUTMENT WP, BURN-OUT COPING, SCREWS, TITANIUM ADHESIVE BASE, ALLIGATOR ABUTMENT, SOLID ABUTMENT, RETENTIVE
K122807 DENTAL IMPLANT SYSTEM
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