510(k) Report

FDA applicant

The Progressive Orthopaedic Company, LLC

North Palm Beach, FL5 decisions2015–20190 recalls

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, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

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

2015: 32016: 12019: 1
2015high 3 (2015) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2015.

FIG. 1 — The Progressive Orthopaedic Company, LLC by year, 2015–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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) Report

Other applicant names beginning “The”

FDA records each applicant name separately; these may or may not be the same firm.