Wenzel Spine

Matched from indexed company URL: WENZEL SPINE

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30061725363006172536Wenzel Spine1N2026-01-012535 Brockton Dr Ste 450 Austin TX US 78758
30080098503008009850WENZEL SPINE, Inc.1N2020-04-251130 Rutherford Lane Suite 200 Austin TX US 78753

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00813210020153VariLift-LX - The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation.855-936-9351info@wenzelspine.com
00813210020160VariLift-LX - The Wenzel Spine VariLift-LX Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-LX is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-LX is designed to be implanted bi-laterally via a PLIF or TLIF approach, and may be implanted with or without supplemental fixation.855-936-9351info@wenzelspine.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2830211918368509K250247panaSIa SI Fusion SystemOUR2025-07-09
2830211214771052K231807primaLOK™ SP Interspinous Fusion SystemPEK2023-08-15
2830211383594176K231076VariLift®-C Interbody Fusion SystemODP2023-09-27
2830211351739311K180822VariLift-LX Interbody Fusion System, VariLift-C Interbody Fusion SystemMAX2019-01-28
2830211670855334K173247Surgical Planning Software version 1.1LLZ2017-11-08
2830211515090828K172327VMA™ System version 3.0LLZ2017-08-25
1100241146917381K151900VariLift-L Interbody Fusion DeviceMAX2015-12-11
1100241520775765K131296VARILIFT-L INTERBODY FUSION DEVICEMAX2013-09-03
1100241452407044K120603VARILIFT -CODP2013-01-29
1100241361512159K111123VARILIFT CERVICAL INTERBODY FUSION SYSTEMODP2011-12-08
1100241983676833K102438PRIMALOK FACET FIXATION SYSTEMMRW2010-09-30
2830211983676833K102438PRIMALOK FACET FIXATION SYSTEMMRW2010-09-30
2830211305169931K100820WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEMMAX2010-08-05
1100241305169931K100820WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEMMAX2010-08-05
1100241613069402K100354PRIMAL OK INTERSPINOUS FUSION SYSTEMKWP2010-08-17
2830211613069402K100354PRIMAL OK INTERSPINOUS FUSION SYSTEMKWP2010-08-17
1100242045541059K030608OTI BONE CEMENT PLUGJDK2003-06-12

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MAX52019-01-28
ODP32023-09-27
LLZ22017-11-08
MRW22010-09-30
KWP22010-08-17
OUR12025-07-09
PEK12023-08-15
JDK12003-06-12

PMN#

GUDID#

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