Clearance Summary
MPa Max adhesive received FDA 510(k) clearance under submission number K262252, sponsored by Den-Mat Holdings, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2026-09-24.
- Submission: K262252
- Applicant / Sponsor: Den-Mat Holdings, LLC
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3200
- Decision date: 2026-09-24
Classification & Regulation
This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.