Ossvis Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K242703LW Pre-milled AbutmentDecember 5, 2024
K242379LL Implant SystemNovember 7, 2024
K233808LW Narrow Implant SystemJuly 31, 2024
K233167LW Implant System – AbutmentMarch 25, 2024
K231235LW UCLA AbutmentSeptember 15, 2023
K231079LW Retraction CapSeptember 14, 2023
K223924LW Implant SystemAugust 8, 2023