Remi Impression Material— 510(k) K251724
Substantially EquivalentGrindguard, Inc.
FDA 510(k) clearance K251724 for Remi Impression Material, Substantially Equivalent on 2026-02-25. Applicant: Grindguard, Inc.. Device class: 2.
Clearance details
- Applicant
- Grindguard, Inc.
- Product code
- Code SHI
- Device class
- Class 2
- Regulation
- 21 CFR 872.3660
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Francisco, CA, US
Recent devices under product code SHI
view allMore clearances from Grindguard, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.