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5 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
CS9600isanextraoralsystemintendedtoproducetwo-dimensionalandthree-dimensionaldigitalX-rayi recall (Z-1627-2023)Trophy SAS2023-05-27
CareStream Dental CS 2100 X-ray system Product Usage: The expected usage (intended use) fo recall (Z-0999-2013)Trophy Sas2013-05-02
CareStream Dental CS 2200 X-ray system Product Usage: The expected usage (intended use) fo recall (Z-1000-2013)Trophy Sas2013-05-02
CareStream Dental Kodak 2100 Intraoral X-ray system Product Usage: The expected usage (int recall (Z-1094-2013)Trophy Sas2013-05-02
CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The expected usage (int recall (Z-1095-2013)Trophy Sas2013-05-02

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