FDA 510(k) Applications Submitted by Peter Lee

FDA 510(k) Number	Submission Date	Device Name	Applicant
K240232	01/29/2024	EK D3.3 and Ultra Wide Implants	Hiossen, Inc.
K241003	04/12/2024	HIOSSEN Pre-milled Abutment (ET Pre-milled Abutment & EK Pre-milled Abutment)	Hiossen, Inc.
K191201	05/06/2019	EM SA Implant System	Hiossen, Inc.
K191751	07/01/2019	EM Provisional	Hiossen, Inc.
K222636	08/31/2022	ET Abutment System	Hiossen Inc.
K233389	10/02/2023	EK Digital Abutments	Hiossen, Inc.
K203360	11/16/2020	EK Implants and Abutments System	Hiossen, Inc.
K183242	11/21/2018	ET IV SA Dental Implants	Hiossen, Inc.
K974441	11/25/1997	SUNGLASSES	HIP SHING FAT CO., LTD.
K083876	12/29/2008	SFI-BAR SYSTEM COMPLETE 2-IMPLANT AND 4-IMPLANT	CENDRES & METAUX SA