FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

TRI Dental Implant System

K Number: K151916 · Decision Dec 18, 2015
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
3
Review Days
158

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Basic Information

Device Name
TRI Dental Implant System
K Number
K151916
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tri Dental Implants Int. AG
Date Received
July 13, 2015
Decision Date
December 18, 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 Tri Dental Implants Int. AG

K Number Device Name
K242661 TRI-matrix® X-Force Implants
K203660 TRI-matrix Implant Line