K243255
- 510(k) number
- K243255
- Device name
- URIS Long Implant & Abutments
- Applicant
- Truabutment, Inc. CA · US
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2025-07-03
- Date received
- 2024-10-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K243255.pdf
Official FDA record: K243255
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.