Truabutment, Inc.
Truabutment, Inc. holds FDA 510(k) medical device clearances, first cleared 2018, most recent 2025, with 1 FDA device recall on record.
Top product codes for Truabutment, Inc.
FDA recalls by Truabutment, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Truabutment, Inc.
- 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
- K191913 — TruAbutment DS
- K183106 — TruAbutment DS
- K171532 — TruBase S
- K172100 — URIS OMNI System
- K172304 — TruAbutment DS
Data sourced from openFDA. This site is unofficial and independent of the FDA.