Stryker Leibinger GmbH & Co KG - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Stryker Leibinger GmbH & Co KG has 21 FDA 510(k) cleared medical devices. Based in Freiburg Im Breisgau, DE.
Latest FDA clearance: Mar 2026. Active since 2009. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Stryker Leibinger GmbH & Co KG Filter by specialty or product code using the sidebar.
21 devices
Cleared
Mar 12, 2026
MEDPOR Customized Implant Kit
General & Plastic Surgery
73d
Cleared
Feb 19, 2026
Spine Guidance 5.4 Software
Orthopedic
93d
Cleared
Feb 06, 2026
Spine Guidance 5.3 Software
Orthopedic
149d
Cleared
Dec 11, 2024
SternalPlate Expansion
Orthopedic
29d
Cleared
Aug 27, 2024
Q Guidance System
Orthopedic
90d
Cleared
Jul 25, 2024
Spine Guidance Software (Version 5.1)
Orthopedic
90d
Cleared
Jul 12, 2024
MRI Universal
Dental
127d
Cleared
Jun 06, 2024
Spine Guidance Software (version 5.0)
Orthopedic
90d
Cleared
Mar 14, 2024
Ortho Guidance Precision Knee Software
Orthopedic
132d
Cleared
Aug 24, 2023
Stryker MP, Mandible, HMMF and MMF AXS Screws
Dental
84d
Cleared
Aug 14, 2023
Stryker Resorbable Fixation System
Neurology
109d
Cleared
Aug 05, 2023
Stryker Resorbable Fixation System
Dental
142d