FloShield, Inc. is one of 16368 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
FloShield, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
FloShield, Inc. has 1 FDA 510(k) cleared medical devices. Based in Weatherford, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by FloShield, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Advance BioReg, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - FloShield, Inc.
1 devices