Haemoband Surgical, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Haemoband Surgical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SleeveLUX 24 Anoscope/Proctoscope (P2001)
2
Total
2
Cleared
0
Denied
Haemoband Surgical, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Bonita Springs, US.
Latest FDA clearance: Oct 2025. Active since 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Haemoband Surgical, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Haemoband Surgical, Ltd.
2 devices