FDA applicant
Medtaxx Partners
FDA records 1 decision for Medtaxx Partners (Crofton, MD) in 2000: 1 510(k) clearance. All are in product code LYY (Latex Patient Examination Glove). 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 Medtaxx Partners’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Medtaxx Partners since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medtaxx Partners’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