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Dynasthetics

US Last updated 23 Oct 2026

Devices
14
Registries
GUDIDFDA 510(k)FDA
FDA recalls
11 ongoing

Catalogue14

FDA recalls1

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

  • 2022

    • 9 May 2022 Z-1591-2023 Class II Ongoing Due to a manufacturing issue that may result in filter leakage.

Information

Country
US
Address
4694 S 200 W, Salt Lake City, UT, 84107
FDA FEI number
3008776780