Hiossen, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ET Healing Abutments, EK MULTI ANGLED 30 ABUTMENT, HIOSSEN Pre-milled Abutment (ET Pre-milled Abutment & EK Pre-milled Abutment)
26
Total
26
Cleared
0
Denied
FDA 510(k) Regulatory Record - Hiossen, Inc. Dental ✕
26 devices
Cleared
May 14, 2026
ET Healing Abutments
Dental
226d
Cleared
Jan 29, 2026
EK MULTI ANGLED 30 ABUTMENT
Dental
266d
Cleared
Jan 08, 2025
HIOSSEN Pre-milled Abutment (ET Pre-milled Abutment & EK Pre-milled Abutment)
Dental
271d
Cleared
Sep 13, 2024
EK D3.3 and Ultra Wide Implants
Dental
228d
Cleared
May 29, 2024
EK Digital Abutments
Dental
240d
Cleared
Apr 28, 2023
ET Abutment System
Dental
240d
Cleared
Jan 07, 2022
EK Implants and Abutments System
Dental
417d
Cleared
Dec 16, 2019
EM Provisional
Dental
168d
Cleared
Nov 15, 2019
EM SA Implant System
Dental
193d
Cleared
May 21, 2019
ET IV SA Dental Implants
Dental
181d
Cleared
May 16, 2018
IS3
Dental
77d
Cleared
Jan 11, 2018
ET Hybrid Abutment
Dental
332d