K251239

GrandioSO Unlimited

510(k) number
K251239
Device name
GrandioSO Unlimited
Applicant
Voco GmbH DE
Product code
EBF — Material, Tooth Shade, Resin
Decision date
2025-05-21
Date received
2025-04-22
Decision
Substantially Equivalent
Clearance type
Special
Advisory committee
Dental
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K251239
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.