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/ Embolx, Inc.
Embolx, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0
Known Names
embolx, embol-x
Recent 510(k) Clearances
K-Number
Device
Date
K232536
Soldier Microcatheter
February 23, 2024
K180904
Sniper Infusion Catheter with Balloon Occlusion
June 8, 2018
K142692
Occlusion Balloon Catheter
May 31, 2015