Skeletal Dynamics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Skeletal Dynamics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Clavicle Fixation System, Geminus Volar Distal Radius Plating System, Proximal Humerus Fixation System
20
Total
20
Cleared
0
Denied
Skeletal Dynamics, Inc. has 20 FDA 510(k) cleared orthopedic devices. Based in Miami, US.
Latest FDA clearance: Mar 2026. Active since 2020.
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 - Skeletal Dynamics, Inc.
20 devices
Cleared
Mar 23, 2026
Clavicle Fixation System
Orthopedic
82d
Cleared
Nov 13, 2025
Geminus Volar Distal Radius Plating System
Orthopedic
58d
Cleared
Nov 14, 2024
Proximal Humerus Fixation System
Orthopedic
90d
Cleared
Nov 01, 2024
Total Wrist Arthroplasty System (TWA)
Orthopedic
2d
Cleared
Sep 26, 2024
Protean Fragment Plating System
Orthopedic
94d
Cleared
Aug 01, 2024
Freefix Forearm Plating System
Orthopedic
17d
Cleared
Jul 19, 2024
Suture Button Repair System
Orthopedic
115d
Cleared
Dec 15, 2023
Double Internal Joint Stabilizer- Elbow
Orthopedic
211d
Cleared
Sep 28, 2023
ALIGN Radial Head System
Orthopedic
155d
Cleared
Aug 28, 2023
Distal Elbow Plating System
Orthopedic
87d
Cleared
May 10, 2023
Internal Joint Stabilizer - Elbow
Orthopedic
194d
Cleared
Apr 28, 2023
Hand Trauma Threaded Nail System
Orthopedic
28d