FDA applicant
Luv N' Care, Ltd.
FDA records 2 decisions for Luv N' Care, Ltd. (Monroe, LA) in 2010: 2 510(k) clearances. Most are in product codes KKO (Ring, Teething, Fluid-Filled) and HGX (Pump, Breast, 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 Luv N' Care, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2010
2010high 2 (2010) · low 0 (2011)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2010.
Planning a device like Luv N' Care, 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