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Freyja Healthcare, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K252640
VereSee Optical Veres Needle and Endoscopic Camera
October 20, 2025
K232464
VereSee Optical Veres Needle System
May 2, 2024