fda
1 records
FDA Device Recall: Erisma- LP posterior fixation system with the below specifically affected produc
2019-07-24
Class III — Potential for the polyaxial screw to become disassembled during implant.
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ny_corps
1 records
NY Corp: CLARIANCE, INC.
2016-07-27
FOREIGN BUSINESS CORPORATION | County: New York | Jurisdiction: Delaware
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