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/ Kane Biotech, Inc.
Kane Biotech, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K252759
revyve® Antimicrobial Skin and Wound Cleanser
January 8, 2026
K241809
coactiv+ Antimicrobial Wound Gel
July 19, 2024
K223259
coactiv+ Antimicrobial Wound Gel
May 24, 2023