K260006
- 510(k) number
- K260006
- Device name
- INOSS System
- Applicant
- Inosys, Inc. NY · US
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2026-06-17
- Date received
- 2026-01-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K260006.pdf
Official FDA record: K260006
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.