Ossvis Co., Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Ossvis Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Anyang-Si, KR.
Latest FDA clearance: Dec 2024. Active since 2023. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ossvis Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Withus Group, Inc. as regulatory consultant.
7 devices
Cleared
Dec 05, 2024
LW Pre-milled Abutment
Dental
87d
Cleared
Nov 07, 2024
LL Implant System
Dental
87d
Cleared
Jul 31, 2024
LW Narrow Implant System
Dental
244d
Cleared
Mar 25, 2024
LW Implant System – Abutment
Dental
180d
Cleared
Sep 15, 2023
LW UCLA Abutment
Dental
140d
Cleared
Sep 14, 2023
LW Retraction Cap
Dental
150d
Cleared
Aug 08, 2023
LW Implant System
Dental
221d