Maxx Orthopedics, Inc.

FDA Regulatory Profile

Maxx Orthopedics, Inc. appears in FDA public data with 0 recalls, 25 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 7, 2026.

Summary

Total Recalls
0
510(k) Clearances
25
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K261563Freedom Total Knee System (E-Poly Tibial Liners)August 7, 2026
K261609Freedom Partial Knee SystemAugust 4, 2026
K253171Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)January 15, 2026
K252777Freedom Metaphyseal Cone Implants (Metaphyseal Cones)October 31, 2025
K253314Freedom Infinia™ Total Knee SystemOctober 29, 2025
K253144Freedom® Total Knee System – Titan PCK ComponentsOctober 22, 2025
K243634Maxx Libertas Bipolar Hip Head (Bipolar Hip)August 25, 2025
K251717Freedom® Total Knee System – Titanium Tibial Base PlateJune 26, 2025
K250382Freedom Total Knee System (All-poly Tibial Plate)March 13, 2025
K241597Freedom® Total Knee System - Porous Tibial Base PlateFebruary 13, 2025
K243277Freedom® Medial Congruent LinerNovember 19, 2024
K240863Freedom® Total Knee SystemJuly 2, 2024
K200912Freedom(R) - TiNbN Coated KneeNovember 18, 2020
K192989Libertas E-XLPE Modular LinerOctober 29, 2020
K192148Freedom Primary PCKSeptember 5, 2019
K183684Libertas – Taper Uncemented Femoral StemAugust 23, 2019
K183365Libertas Acetabular Hooded LinerFebruary 22, 2019
K182574Freedom Ultra-Congruent CR Tibial LinerJanuary 22, 2019
K180973Libertas Hip Replacement SystemSeptember 28, 2018
K150680Freedom Cementless Femoral ComponentJune 26, 2015