Microport Orthopedics, Inc. is one of 25889 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microport Orthopedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NEXUS® Hip Stem, EVOLUTION® AM BIOFOAM® Tibial System, NEXUS® Hip Stem
39
Total
39
Cleared
0
Denied
Microport Orthopedics, Inc. has 39 FDA 510(k) cleared orthopedic devices. Based in Arlington, US.
Latest FDA clearance: Oct 2026. Active since 2014.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Microport Orthopedics, Inc.
39 devices
Cleared
Oct 01, 2026
NEXUS® Hip Stem
Orthopedic
76d
Cleared
Aug 21, 2026
EVOLUTION® AM BIOFOAM® Tibial System
Orthopedic
270d
Cleared
May 15, 2025
NEXUS® Hip Stem
Orthopedic
90d
Cleared
Feb 18, 2025
Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and...
Orthopedic
91d
Cleared
Apr 12, 2024
Ceramic Femoral Head
Orthopedic
57d
Cleared
Apr 01, 2024
EVOLUTION® Hinge Knee System
Orthopedic
87d
Cleared
Jan 18, 2024
EVOLUTION® Tibial Cones
Orthopedic
79d
Cleared
Oct 31, 2023
EVOLUTION® Cement Keel
Orthopedic
123d
Cleared
Sep 27, 2023
EVOLUTION® Hinge Knee System
Orthopedic
210d
Cleared
Jan 05, 2022
MPO Hip Instruments
Orthopedic
29d
Cleared
Jan 05, 2022
MPO Knee Instruments
Orthopedic
29d
Cleared
Oct 01, 2021
E-CLASS® DUAL MOBILITY INSERTS and DYNASTY® DUAL MOBILITY LINERS
Orthopedic
638d
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