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/ Xelite Biomed , Ltd.
Xelite Biomed , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K251896
XeliteMed SuperM-Fix Spinal Bone Cement
January 28, 2026
K243537
XeliteMed VertehighFix High Viscosity Spinal Bone Cement System
April 11, 2025
K241775
XeliteMed VertehighFix High Viscosity Spinal Bone Cement
September 18, 2024