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Exo, Inc.

5 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
Lung AI (LAI001) (K243239)Exo, Inc.2025-04-24
Strain AI (SAI001) (K242359)Exo, Inc.2024-11-20
AI Platform (AIP001) (K232501)Exo, Inc.2023-11-17
Bladder AI (AIBV01) (K230497)Exo, Inc.2023-06-22
HEMOCLAV VENOUS CATHETER (K831801)Exo, Inc.1983-07-07

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Every clearance here is in the API, with alerts when new ones post.