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

URIS OMNI System

K Number: K172100 · Decision May 4, 2018
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
15
Review Days
297

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Basic Information

Device Name
URIS OMNI System
K Number
K172100
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Truabutment, Inc.
Date Received
July 11, 2017
Decision Date
May 4, 2018
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 Truabutment, Inc.

K Number Device Name
K243255 URIS Long Implant & Abutments
K241485 TruAbutment DS; TruBase
K230438 URIS Smart Path Implant System & Prosthetic
K231874 AOT & T-L Abutment
K213961 TruAbutment DS, TruBase
K203649 TruAbutment DS, TruBase
K202579 TruAbutment DS, TruBase
K201842 TruBase S
K201197 TruAbutment DS, TruBase S
K200817 URIS OMNI Narrow System & Prosthetic
Search all 15 clearances from Truabutment, Inc. →