Ossvis Co., Ltd.

7 FDA 510(k) medical device clearances.

Top product codes for Ossvis Co., Ltd.

NHA — Dental 4 devices
DZE — Dental 3 devices

Recent clearances by Ossvis Co., Ltd.

K242703 — LW Pre-milled Abutment NHA · 2024-12-05
K242379 — LL Implant System DZE · 2024-11-07
K233808 — LW Narrow Implant System DZE · 2024-07-31
K233167 — LW Implant System Abutment NHA · 2024-03-25
K231235 — LW UCLA Abutment NHA · 2023-09-15
K231079 — LW Retraction Cap NHA · 2023-09-14
K223924 — LW Implant System DZE · 2023-08-08

Data sourced from openFDA. This site is unofficial and independent of the FDA.