Pro Lift

GUDID 00190837021535

Life Spine, Inc.

Metallic spinal fusion cage, non-sterile
Primary Device ID00190837021535
NIH Device Record Key0c983a06-91f0-4684-8d9a-b1deaeae86ae
Commercial Distribution StatusIn Commercial Distribution
Brand NamePro Lift
Version Model Number58-1228-0710P
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
GS100190837021535 [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 Date2018-09-03
Device Publish Date2018-08-01

On-Brand Devices [Pro Lift]

0019083702161058-1228-0708P
0019083702153558-1228-0710P
0019083702150458-1228-0813P
00190837030940151-261
001908370910332019-0080
00190837091026129-1018
00190837091019129-1017

Trademark Results [Pro Lift]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PRO LIFT
PRO LIFT
97404686 not registered Live/Pending
Nielsen Products, LLC
2022-05-11
PRO LIFT
PRO LIFT
86190353 4620199 Live/Registered
Nielsen Products, LLC
2014-02-11
PRO LIFT
PRO LIFT
85824793 not registered Dead/Abandoned
Nielsen Products, LLC
2013-01-16
PRO LIFT
PRO LIFT
76266174 2644287 Dead/Cancelled
Loren S. Fond, Inc.
2001-06-01
PRO LIFT
PRO LIFT
75596156 not registered Dead/Abandoned
HUFFY CORPORATION
1998-11-19
PRO LIFT
PRO LIFT
73506693 1340578 Dead/Cancelled
ANDERSON, HAROLD R.
1984-11-01

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