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Serpex Medical, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K252874
Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01
October 8, 2025
K221206
Compass Steerable Needle
August 25, 2022
K221302
Recon Steerable Sheath
August 15, 2022