K251724
- 510(k) number
- K251724
- Device name
- Remi Impression Material
- Applicant
- Grindguard, Inc. CA · US
- Product code
- SHI — Impression Material For Fabrication Of Patient-Match
- Decision date
- 2026-02-25
- Date received
- 2025-06-04
- 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: K251724.pdf
Official FDA record: K251724
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.