Inion OY - FDA 510(k) Cleared Devices
14
Total
13
Cleared
0
Denied
Inion OY has 13 FDA 510(k) cleared orthopedic devices. Based in Tampere, FI.
Latest FDA clearance: Nov 2025. Active since 2005.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Nov 07, 2025
Inion CPS 1.5 Baby Bioabsorbable Fixation System
Dental
182d
Cleared
Jul 11, 2025
Inion CPS 1.5/2.0/2.5 Bioabsorbable Fixation System
Neurology
59d
Cleared
Jan 13, 2021
Inion CompressOn Screw
Orthopedic
90d
Cleared
Jul 31, 2019
Inion BioRestore
Orthopedic
30d
Cleared
Oct 06, 2015
Inion Spinal Graft Containment System
Orthopedic
139d
Cleared
Apr 11, 2014
INION FREEDOMPIN
Orthopedic
109d
Cleared
Feb 27, 2013
INION FREEDOMSCREW (ALTERNATIVE MARKETING NAME: INION OTPS FREEDOMSCREW)
Orthopedic
90d
Cleared
Jan 29, 2013
INION CPS ORBITAL PLATES
Dental
131d
Cleared
Feb 20, 2009
INION BIORESTORE BIODEGRADABLE BONE GRAFT SUBSTITUTE
Orthopedic
28d
Cleared
Oct 11, 2007
INION BIORESTORE
Orthopedic
185d
Cleared
Aug 03, 2007
INION HEXALON BIODEGRADABLE ACL/PCL SCREW
Orthopedic
66d
Cleared
Jul 24, 2007
INION BIORESTORE
Dental
125d
Cleared
Nov 09, 2006
INION ANCHRON PLUS BIODEGRADABLE ANCHOR SYSTEM, MODEL ANC-6001
Orthopedic
52d
Cleared
Aug 04, 2005
INION ANCHRON BIODEGRADABLE ANCHOR SYSTEM, MODEL ANC-6000
Orthopedic
71d