fda
3 records
FDA Device Recall: Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog Number:
2025-12-24
Class II — Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
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FDA Device Recall: Brand Name: AART Malar Implant Product Name: Malar Implant Model/Catalog Numbe
2025-12-24
Class II — Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
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FDA Device Recall: Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant
2025-12-24
Class II — Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.
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ny_corps
1 records
NY Corp: DSAART LLC
2019-02-21
DOMESTIC LIMITED LIABILITY COMPANY | County: New York | Jurisdiction: New York
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