FDA 510(k) Application Details - K222581

Device Classification Name	Material, Tooth Shade, Resin   More FDA Info for this Device
510(K) Number	K222581
Device Name	Material, Tooth Shade, Resin
Applicant	SDI Limited 3-15 Brunsdon Street, Bayswater Melbourne 3153 AU Other 510(k) Applications for this Company
Contact	Quynh Jewell Other 510(k) Applications for this Contact
Regulation Number	872.3690   More FDA Info for this Regulation Number
Classification Product Code	EBF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/26/2022
Decision Date	10/28/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review