FDA applicant
Shanghai Poseidon Plastic Products Co., Ltd.
FDA records 8 decisions for Shanghai Poseidon Plastic Products Co., Ltd. (Sparks, NV) from 1995 to 2000: 8 510(k) clearances. Most are in product codes LZA (Polymer Patient Examination Glove) and LYZ (Vinyl Patient Examination Glove). 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 Shanghai Poseidon Plastic Products Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Shanghai Poseidon Plastic Products Co., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Shanghai Poseidon Plastic Products…’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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