FDA applicant
The Progressive Orthopaedic Company, LLC
FDA records 5 decisions for The Progressive Orthopaedic Company, LLC (North Palm Beach, FL) from 2015 to 2019: 5 510(k) clearances. Most are in product codes JWH (Prosthesis, Knee, Patellofemorotibial…) and LPH (Prosthesis, Hip, Semi-Constrained…). Its devices cite 8 predicates, 4 of them its own earlier devices. 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 The Progressive Orthopaedic Company, LLC’s devices, and how often a recall has named them.
FDA decisions per year
1in 2019
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2015.
Planning a device like The Progressive Orthopaedic Company, LLC’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) ReportOther applicant names beginning “The”
FDA records each applicant name separately; these may or may not be the same firm.