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Exo, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243239Lung AI (LAI001)April 24, 2025
K242359Strain AI (SAI001)November 20, 2024
K232501AI Platform (AIP001)November 17, 2023
K230497Bladder AI (AIBV01)June 22, 2023
K831801HEMOCLAV VENOUS CATHETERJuly 7, 1983