FDA applicant
Poirier S.A.
FDA records 17 decisions for Poirier S.A. (Mchenry, IL) in 1984: 17 510(k) clearances. Most are in product codes IQC (Wheelchair, Special Grade) and IOR (Wheelchair, Mechanical). 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 Poirier S.A.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Poirier S.A. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Poirier S.A.’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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