Bonalive Biomaterials, Ltd.

FDA Regulatory Profile

Bonalive Biomaterials, Ltd. has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jul 11, 2023

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances2Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K231528Bonalive Orthopedics granulesJul 11, 2023
K191274BonAlive GranulesAug 7, 2019