Safepath Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Safepath Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SafePath Sulturing System-Silk Suture, SafePath Sulturing System Polyamide Suture (Nylon) SafePath Sulturing System- Polypropylene Suture, SafePath Suturing System
2
Total
2
Cleared
0
Denied
Safepath Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Amesbury, US.
Latest FDA clearance: Oct 2024. Active since 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Safepath Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Safepath Medical, Inc.
2 devices