Kane Biotech, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Kane Biotech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: revyve® Antimicrobial Skin and Wound Cleanser, coactiv+™ Antimicrobial Wound Gel, coactiv+™ Antimicrobial Wound Gel
3
Total
3
Cleared
0
Denied
Kane Biotech, Inc. has 3 FDA 510(k) cleared medical devices. Based in Winnipeg, CA.
Latest FDA clearance: Jan 2026. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kane Biotech, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Albert Rego, PhD, Inc. and Acostar Limited.
FDA 510(k) Regulatory Record - Kane Biotech, Inc.
3 devices