Borze, Inc. is one of 26054 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Borze, Inc. - FDA 510(k) Cleared Devices
Recent clearances: B`orze Inc Laser Family (Sorren/Adonis)
1
Total
1
Cleared
0
Denied
Borze, Inc. has 1 FDA 510(k) cleared medical devices. Based in Boise, US.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Borze, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shenzhen Hlongmed Biotech Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Borze, Inc.
1 devices