K233389
- 510(k) number
- K233389
- Device name
- EK Digital Abutments
- Applicant
- Hiossen, Inc. PA · US
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-05-29
- Date received
- 2023-10-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K233389.pdf
Official FDA record: K233389
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.