Medical Device Manufacturer · US , Austin , TX

Wenzel Spine, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2013
6
Total
6
Cleared
0
Denied

Wenzel Spine, Inc. has 6 FDA 510(k) cleared medical devices. Based in Austin, US.

Latest FDA clearance: Jul 2025. Active since 2013. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Wenzel Spine, Inc. Filter by specialty or product code using the sidebar.

6 devices
1–6 of 6
panaSIa SI Fusion System
K250247 · OUR Sacroiliac Joint Fixation · Orthopedic
Jul 2025 163d
VariLift?-C Interbody Fusion System
K231076 · ODP Intervertebral Fusion Device With Bone Graft, Cervical · Orthopedic
Sep 2023 166d
primaLOK? SP Interspinous Fusion System
K231807 · PEK Spinous Process Plate · Orthopedic
Aug 2023 56d
VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion System
K180822 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar · Orthopedic
Jan 2019 304d
VariLift-L Interbody Fusion Device
K151900 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar · Orthopedic
Dec 2015 154d
VARILIFT-L INTERBODY FUSION DEVICE
K131296 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar · Orthopedic
Sep 2013 120d
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