FDA applicant
Riancorp Pty, Ltd.
FDA records 1 decision for Riancorp Pty, Ltd. (Leesburg, FL) in 2004: 1 510(k) clearance. All are in product code NZY (Light, Lymphedema Reduction, Low Energy). 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 Riancorp Pty, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Riancorp Pty, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Riancorp Pty, 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