FDA applicant
Vitaid, Ltd.
FDA records 7 decisions for Vitaid, Ltd. (Ontario, Canada, CA) from 1989 to 2005: 7 510(k) clearances. Most are in product codes BTR (Tube, Tracheal (W/Wo Connector)) and EZL (Catheter, Retention Type, Balloon). Its devices cite 1 predicate, 0 of them its own earlier devices. 3 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Vitaid, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Vitaid, Ltd. since 2007.
Recalls per year
2in 2007
Class I Class II/III not classified
Planning a device like Vitaid, 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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