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Preat Corporation
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K243824
Preat Abutments
May 8, 2025
K220823
Preat Abutments
October 26, 2022
K183518
Preat Abutments
March 18, 2019