Inion , Ltd. - FDA 510(k) Cleared Devices
23
Total
22
Cleared
0
Denied
Inion , Ltd. has 22 FDA 510(k) cleared medical devices. Based in Tampere, FI.
Historical record: 22 cleared submissions from 2001 to 2008. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Inion , Ltd. Filter by specialty or product code using the sidebar.
23 devices
Cleared
Jul 11, 2008
INION SPINAL GRAFT CONTAINMENT SYSTEM
Orthopedic
375d
Cleared
Jan 23, 2007
INION CPS/OTPS FREEDOMPLATE
Orthopedic
71d
Cleared
Oct 04, 2006
MODIFICATION TO INION OTPS BIODEGRADABLE FIXATION SYSTEM
Orthopedic
29d
Cleared
Mar 13, 2006
INION HEXALON BIODEGRADABLE ACL/PCL SCREW
Orthopedic
26d
Cleared
Nov 25, 2005
INION S-1 BIODEGRADABLE ANTERIOR CERVICAL FUSION SYSTEM
Orthopedic
143d
Cleared
Nov 16, 2005
INION OTPS BIODEGRADABLE DISTAL RADIUS PLATE
Orthopedic
54d
Cleared
Sep 20, 2005
INION CPS BABY 1.5 BIOABSORBABLE FIXATION SYSTEM
Dental
14d
Cleared
May 27, 2005
INION CPS BABY 1.5 BIOABSORBABLE FIXATION SYSTEM, 40 AND 64 HOLE PLATES,...
Dental
4d
Cleared
Mar 07, 2005
MODIFICATION TO: INION OTPS BIODEGRADABLE PIN
Orthopedic
28d
Cleared
Feb 18, 2005
INION OTPS BIODEGRADABLE MINI PLATING SYSTEM
Orthopedic
95d
Cleared
Aug 16, 2004
INION TRINION BIODEGRADABLE MENISCUS SCREW
Orthopedic
441d
Cleared
Mar 31, 2004
INION GTR BIODEGRADABLE MEMBRANE SYSTEM
Dental
184d