ProLift® Expandable Spacer System

GUDID 00190837202255

Life Spine, Inc.

Metallic spinal interbody fusion cage
Primary Device ID00190837202255
NIH Device Record Key6826beeb-460f-4ea6-ba4f-080bde124739
Commercial Distribution StatusIn Commercial Distribution
Brand NameProLift® Expandable Spacer System
Version Model Number67-1028-1208
Company DUNS183641617
Company NameLife Spine, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100190837202255 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-01-19
Device Publish Date2026-01-09

On-Brand Devices [ProLift® Expandable Spacer System]

0019083715663366-1036-0915
0019083715662666-1036-0912
0019083715661966-1036-0907
0019083715660266-1036-0900
0019083715659666-1036-0815
0019083715658966-1036-0812
0019083715657266-1036-0807
0019083715656566-1036-0800
0019083715655866-1031-1215
0019083715654166-1031-1212
0019083715653466-1031-1207
0019083715652766-1031-1200
0019083715650366-1031-1012
0019083715649766-1031-1007
0019083715648066-1031-1000
0019083715647366-1031-0915
0019083715646666-1031-0912
0019083715645966-1031-0907
0019083715644266-1031-0900
0019083715643566-1031-0815
0019083715642866-1031-0812
0019083715641166-1031-0807
0019083715640466-1031-0800
0019083715639866-1026-1215
0019083715638166-1026-1212
0019083715637466-1026-1207
0019083715636766-1026-1200
0019083715635066-1026-1015
0019083715634366-1026-1012
0019083715633666-1026-1007
0019083715632966-1026-1000
0019083715631266-1026-0915
0019083715630566-1026-0912
0019083715629966-1026-0807
0019083715628266-1026-0900
0019083715627566-1026-0815
0019083715626866-1026-0812
0019083715625166-1026-0807
0019083715624466-1026-8000
0019083720469367-1236-1015
0019083720468667-1236-1510
0019083720467967-1236-1508
0019083720466267-1236-1210
0019083720465567-1236-1208
0019083720464867-1236-0813
0019083720463167-1236-0710
0019083720462467-1236-0708
0019083720461767-1234-1015
0019083720460067-1234-1510

Trademark Results [ProLift]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PROLIFT
PROLIFT
88481969 not registered Live/Pending
Waterrox Investments, LLC
2019-06-20
PROLIFT
PROLIFT
87271661 not registered Live/Pending
Seville Classics Inc.
2016-12-16
PROLIFT
PROLIFT
86599032 4855635 Live/Registered
EGYED DESTINY
2015-04-15
PROLIFT
PROLIFT
86574562 5319833 Live/Registered
Toyota Material Handling Midwest, Inc.
2015-03-24
PROLIFT
PROLIFT
86574549 5319832 Live/Registered
Toyota Material Handling Midwest, Inc.
2015-03-24
PROLIFT
PROLIFT
86572881 5211561 Live/Registered
Toyota Material Handling Midwest, Inc.
2015-03-23
PROLIFT
PROLIFT
86572878 5207129 Live/Registered
Toyota Material Handling Midwest, Inc.
2015-03-23
PROLIFT
PROLIFT
86563074 4947699 Live/Registered
Rocky Mountain Vacuum Brokers LLC
2015-03-13
PROLIFT
PROLIFT
86538320 4949158 Live/Registered
Toyota Material Handling Midwest, Inc.
2015-02-18
PROLIFT
PROLIFT
86340264 4811118 Live/Registered
Safe-T-Shade, Inc.
2014-07-17
PROLIFT
PROLIFT
86238663 4783625 Live/Registered
Beaty, Mark M.
2014-04-01
PROLIFT
PROLIFT
85435041 not registered Dead/Abandoned
Handy Button Machine Co.
2011-09-29
© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.