Coloplast is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Coloplast - FDA 510(k) Cleared Devices
Recent clearances: Luja female (20051), Virtue Male Sling System with Alexis Wound Retractor Convenience Kit, Luja Coudé (20118 Male CH8 - small packaging (Pocket size)), Luja Coudé (20111 Male CH10 - small packaging (Pocket size)), Luja Coudé (20112 Male CH12 - small packaging (Pocket size)), Luja Coudé (20114 Male CH14 - small packaging (Pocket size)), Luja Coudé (20101 Male CH10 - large packaging), Luja Coudé (20102 Male CH12 - large packaging), Luja Coudé (20104 Male CH14 - large packaging), Luja Coudé (20106 Male CH16 - large packaging)
Coloplast has 14 FDA 510(k) cleared gastroenterology & urology devices. Based in Plymouth, US.
Latest FDA clearance: Jul 2024. Active since 2018.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.