FDA applicant
Jri Manufacturing, Ltd.
FDA records 1 decision for Jri Manufacturing, Ltd. (Crofton, MD) in 2004: 1 510(k) clearance. All are in product code MEH (Prosthesis, Hip, Semi-Constrained, Uncemented…). 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 Jri Manufacturing, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Jri Manufacturing, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Jri Manufacturing, 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