FDA applicant
Synmertex Co, Ltd.
FDA records 5 decisions for Synmertex Co, Ltd. (Rowland Heights, CA) in 2003: 5 510(k) clearances. All are in product code 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 Synmertex Co, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Synmertex Co, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Synmertex 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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