fda
2 records
FDA Device Recall: TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
2025-11-26
Class I — Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position.
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FDA Device Recall: Stryker TMJ Unilateral Implant, REF: GHG010, consisting of the following compon
2024-10-02
Class II — Patient-fitted temporomandibular (TMJ) prothesis contained incorrect components, SterileEO
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ny_corps
1 records
NY Corp: TMJ SOLUTIONS, LLC
2019-04-10
DOMESTIC LIMITED LIABILITY COMPANY | County: Schenectady | Jurisdiction: New York
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