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Home
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Lincotek Medical
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
10
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K252081
SportLinc Syndesmosis Device
March 27, 2026
K250764
SpineLinc Anterior Cervical Implant System
December 5, 2025