Extremity Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Extremity Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: MetaFore Small Screw System, Extremity Medical External Fixation System, Extremity Medical External Fixation System
28
Total
28
Cleared
0
Denied
Extremity Medical, LLC has 28 FDA 510(k) cleared orthopedic devices. Based in Parsippany, US.
Latest FDA clearance: Oct 2025. Active since 2008.
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 - Extremity Medical, LLC
28 devices
Cleared
Oct 08, 2025
MetaFore Small Screw System
Orthopedic
226d
Cleared
May 07, 2025
Extremity Medical External Fixation System
Orthopedic
26d
Cleared
Feb 21, 2025
Extremity Medical External Fixation System
Orthopedic
266d
Cleared
Aug 20, 2021
Omni Foot and Ankle Plating System
Orthopedic
29d
Cleared
May 28, 2021
Axis Charcot Fixation System
Orthopedic
32d
Cleared
Jul 08, 2020
Intraosseous Fixation System
Orthopedic
28d
Cleared
Mar 04, 2020
KinematX Total Wrist Arthroplasty System
Orthopedic
268d
Cleared
Nov 21, 2019
Axis Plating System
Orthopedic
62d
Cleared
May 23, 2018
AlignX Ankle Fusion System
Orthopedic
30d
Cleared
May 22, 2018
Omni Foot Plating System
Orthopedic
55d
Cleared
Nov 06, 2017
Omni Foot Plating System
Orthopedic
102d
Cleared
Jul 13, 2017
Axis Charcot Fixation System, 4.5 to 8.5mm Screw System
Orthopedic
99d