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

TruAbutment DS, TruBase

K Number: K213961 · Decision Jul 14, 2022
Classifications
1
FEI Numbers
390
Registration Numbers
390
Same Product Code
672
Applicant Total
15
Review Days
206

Basic Information

Device Name
TruAbutment DS, TruBase
K Number
K213961
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
TruAbutment Inc.
Date Received
December 20, 2021
Decision Date
July 14, 2022
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

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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
K203649 TruAbutment DS, TruBase
K202579 TruAbutment DS, TruBase
K201842 TruBase S
K201197 TruAbutment DS, TruBase S
K200817 URIS OMNI Narrow System & Prosthetic
K191913 TruAbutment DS
Search all 15 clearances from TruAbutment Inc. →