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

URIS Long Implant & Abutments

K Number: K243255 · Decision Jul 3, 2025
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
15
Review Days
261

Basic Information

Device Name
URIS Long Implant & Abutments
K Number
K243255
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
October 15, 2024
Decision Date
July 3, 2025
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 TruAbutment Inc.

K Number Device Name
K241485 TruAbutment DS; TruBase
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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
K191913 TruAbutment DS
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