K252430

Freeprint® denture flex

510(k) number
K252430
Device name
Freeprint® denture flex
Applicant
Detax GmbH DE
Product code
EBI — Resin, Denture, Relining, Repairing, Rebasing
Decision date
2025-10-30
Date received
2025-08-01
Decision
Substantially Equivalent
Clearance type
Traditional
Advisory committee
Dental
510(k) Summary (official FDA PDF): K252430.pdf
Official FDA record: K252430
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.