FDA applicant
Puronxy, Inc.
FDA records 1 decision for Puronxy, Inc. (San Diego, CA) in 2006: 1 510(k) clearance. All are in product code NXH (Nursing Pad, Cohesive Gel). 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 Puronxy, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Puronxy, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Puronxy, Inc.’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