FDA applicant
Alshifa Medical Syringes Mfg. Co., Ltd.
FDA records 2 decisions for Alshifa Medical Syringes Mfg. Co., Ltd. (Great Neck,, NY) in 1997: 2 510(k) clearances. All are in product code FMF (Syringe, Piston). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Alshifa Medical Syringes Mfg. Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Alshifa Medical Syringes Mfg. Co., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Alshifa Medical Syringes Mfg. Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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