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Safepath Medical, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K222944
SafePath Sulturing System-Silk Suture, SafePath Sulturing System Polyamide Suture (Nylon) SafePath S
October 18, 2024
K180701
SafePath Suturing System
June 25, 2018