K252727
- 510(k) number
- K252727
- Device name
- Neodent InLab Validated Workflow
- Applicant
- JJGC Indústria e Comércio de Materiais Dentários S.A. BR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2026-01-07
- Date received
- 2025-08-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252727.pdf
Official FDA record: K252727
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.