Medartis AG - FDA 510(k) Cleared Devices
Recent clearances: APTUS Clavicle System 2.8, TITAN Nail, APTUS Shoulder Proximal Humerus System, PentaLock 3.5
42
Total
42
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medartis AG Orthopedic ✕
38 devices
Cleared
Jun 05, 2026
APTUS Clavicle System 2.8
Orthopedic
88d
Cleared
Apr 17, 2026
TITAN Nail
Orthopedic
28d
Cleared
Mar 16, 2026
APTUS Shoulder Proximal Humerus System, PentaLock 3.5
Orthopedic
98d
Cleared
Mar 07, 2025
APTUS Hand System
Orthopedic
105d
Cleared
Jun 20, 2024
APTUS Elbow Dorsal Olecranon Plates
Orthopedic
107d
Cleared
Apr 19, 2024
APTUS Foot System 2.8-3.5
Orthopedic
280d
Cleared
Mar 21, 2024
APTUS Hand Scaphoid Plates
Orthopedic
90d
Cleared
Nov 03, 2023
APTUS Cannulated Compression Screws Line Extension, APTUS K-Wire System Line...
Orthopedic
98d
Cleared
Aug 18, 2023
Sterile Products of the APTUS System
Orthopedic
30d
Cleared
Jun 02, 2023
APTUS® 3.5 TriLock Straight Plates
Orthopedic
58d
Cleared
Mar 30, 2023
Medartis APTUS® Ulna Plates
Orthopedic
97d
Cleared
Mar 26, 2020
APTUS® Ankle Trauma System 2.8/3.5
Orthopedic
90d
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