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Feops NV
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K250635
FEops HEARTguide Simulation Application
November 25, 2025
K223855
FEops HEARTguideTM, FEops HEARTguideTM ALPACA
June 6, 2023
K214066
FEops HEARTguide
February 25, 2022
DEN200030
FEops HEARTguide
September 8, 2021