fda
1 records
FDA Device Recall: 8mm FlexDex Needle Driver, Product Code FD-335 ND
2022-02-02
Class II — The firm is reinforcing the IFU instructions: "Do not use if the package is damaged." If upon inspection of the packaging, any damage is observed, including pinholes or tears in the pouch, ...
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ny_corps
1 records
NY Corp: FLEXDEX INC
2014-03-18
DOMESTIC BUSINESS CORPORATION | County: Rockland | Jurisdiction: New York
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