Medos International SARL - FDA 510(k) Cleared Devices
Recent clearances: CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody, SYMPHONY Navigation Ready Instruments, TriALTIS™ Spine System
97
Total
97
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medos International SARL Orthopedic ✕
76 devices
Cleared
May 26, 2026
CROSSNAV Navigation Enabled Instruments for Disc Preparation and Interbody
Orthopedic
155d
Cleared
Mar 27, 2026
SYMPHONY Navigation Ready Instruments
Orthopedic
60d
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
Jan 19, 2023
TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN...
Orthopedic
111d
Cleared
Oct 18, 2022
TELIGEN System
Orthopedic
302d
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