Medical Device Manufacturer · US , Arlington , TN

Microport Orthopedics, Inc. - FDA 510(k) Cleared Devices

37 submissions · 37 cleared · Since 2014

Total

Cleared

Denied

Microport Orthopedics, Inc. has 37 FDA 510(k) cleared orthopedic devices. Based in Arlington, US.

Latest FDA clearance: May 2025. 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) cleared devices by Microport Orthopedics, Inc.

37 devices

1-12 of 37

Evolution® Total Knee Systems - Kinematic Alignment Instrumentation and...

EVOLUTION® Hinge Knee System

K240043 · KRO

Orthopedic · 87d

Cleared Jan 18, 2024

EVOLUTION® Tibial Cones

K233507 · MBH

Orthopedic · 79d

Cleared Oct 31, 2023

EVOLUTION® Cement Keel

K231947 · JWH

Orthopedic · 123d

Cleared Sep 27, 2023

EVOLUTION® Hinge Knee System

E-CLASS® DUAL MOBILITY INSERTS and DYNASTY® DUAL MOBILITY LINERS

K200011 · LPH

Orthopedic · 638d

Cleared Aug 24, 2021

Prime BIOFOAM® Multi-Hole Shells

K201157 · MBL

Orthopedic · 481d

Cleared Aug 20, 2021

Prime and DYNASTY® Additive Manufacturing Shells

K202705 · OQG

Orthopedic · 338d

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Microport Orthopedics, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Microport Orthopedics, Inc.

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