Medos International SARL - FDA 510(k) Cleared Devices
95
Total
95
Cleared
0
Denied
Medos International SARL has 95 FDA 510(k) cleared orthopedic devices. Based in Raynham, US.
Latest FDA clearance: Oct 2025. Active since 2010.
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 Medos International SARL
95 devices
Cleared
Oct 21, 2025
TriALTIS™ Spine System
Orthopedic
22d
Cleared
Jan 17, 2025
TriALTIS™ Spine System
Orthopedic
98d
Cleared
Sep 16, 2024
CROSSNAV Navigation Enabled Instruments and UNAS Navigation Arrays
Orthopedic
80d
Cleared
Sep 09, 2024
TriALTIS™ Spine System
Orthopedic
59d
Cleared
Dec 12, 2023
TriALTIS™ Spine System
Orthopedic
26d
Cleared
Nov 09, 2023
SYMPHONY OCT System
Orthopedic
38d
Cleared
Oct 06, 2023
2.7 mm GRYPHON™ Flex Knotless PEEK Anchor
Orthopedic
50d
Cleared
Sep 22, 2023
TriALTIS Spine System
Orthopedic
123d
Cleared
Feb 10, 2023
TELIGEN System Peripheral Motor Nerve Stimulation Indications
Neurology
88d
Cleared
Jan 19, 2023
TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN...
Orthopedic
111d
Cleared
Oct 18, 2022
TELIGEN System
Orthopedic
302d
Cleared
Oct 13, 2022
EXPEDIUM® Spine System, EXPEDIUM VERSE® Spine System: ALTALYNE™ Ultra Rods
Orthopedic
58d
Looking for a specific device from Medos International SARL? Search by device name or K-number.
Search all Medos International SARL devices