FDA applicant
Vessa, Ltd.
FDA records 4 decisions for Vessa, Ltd. (Gu34 2p4 England, GB) from 1980 to 1985: 4 510(k) clearances. All are in product code ITI (Wheelchair, Powered). 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 Vessa, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Vessa, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Vessa, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report