FDA 510(k) Application Details - K223706

Device Classification Name	Crown And Bridge, Temporary, Resin   More FDA Info for this Device
510(K) Number	K223706
Device Name	Crown And Bridge, Temporary, Resin
Applicant	Huliang(shanghai) Bio-Tech Co., Ltd. Room 303, Building 5, Lane2388, Xiu Pu Road, Pudong Shanghai CN Other 510(k) Applications for this Company
Contact	Quansheng Wang Other 510(k) Applications for this Contact
Regulation Number	872.3770   More FDA Info for this Regulation Number
Classification Product Code	EBG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/12/2022
Decision Date	05/12/2023
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