ProLift Wedge

ProLift Wedge is an expandable titanium alloy lumbar interbody spacer with adjustable lordosis from 0 to 15 degrees. Its upper and lower teeth contact the vertebral bodies to resist…

Registry build 21.09.26

ProLift Wedge is an expandable titanium alloy lumbar interbody spacer with adjustable lordosis from 0 to 15 degrees. Its upper and lower teeth contact the vertebral bodies to resist rotation and migration. The implant has space for autograft or cancellous or corticocancellous allogeneic bone graft.

The system is intended for skeletally mature patients with degenerative disc disease at one or two contiguous levels from L2 to S1 after six months of nonoperative treatment. Up to Grade 1 spondylolisthesis may be present. Cleared supplemental lumbosacral fixation is required.

Supply and Compatibility

Implants are provided sterile for single use. Different footprints and sizes allow selection for anatomy, while the expansion adjusts the lordotic configuration. Components must not be combined with another system or manufacturer, and the graft and supplemental fixation remain part of the fusion procedure.

14manufacturers in China registered for this device type
49catalogue numbers in this listing
33510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (6), Shandong (2), Shanghai (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MAX
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shanghai Reach Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 30
Changzhou Geasure Medical Apparatus AND Instruments Co., Ltd. Changzhou Jiangsu Contract manufacturer 25
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Showing 12 of 14. All 14 manufacturers in China registered for Intervertebral Fusion Device With Bone Graft, Lumbar

Record

Regulatory record for ProLift Wedge
Listed by Life Spine, United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Manufacturer
510(k) K203361
Record published 2022-11-21
Record revised 2026-01-08 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for ProLift Wedge
Catalogue number Size Status
L114-280-2 In distribution
L129-519 In distribution
70-0828-0815 In distribution
L129-512 In distribution
70-1228-1615 In distribution
70-1228-0815 In distribution
70-1028-1315 In distribution
70-1028-1415 In distribution
70-1228-1215 In distribution
70-0828-1215 In distribution
70-1228-1015 In distribution
114-280-2 In distribution
70-1028-1515 In distribution
70-1028-1015 In distribution
L129-516 In distribution
L180-104 In distribution
70-1228-1415 In distribution
L129-514 In distribution
70-1028-1115 In distribution
114-280-4 In distribution
70-0828-1315 In distribution
70-1028-1215 In distribution
L129-511 In distribution
70-0828-1015 In distribution
180-102 In distribution
114-280-5 In distribution
70-1028-1615 In distribution
L129-513 In distribution
70-1028-0815 In distribution
180-104 In distribution
L180-103 In distribution
70-1028-0915 In distribution
70-0828-0915 In distribution
L114-280-4 In distribution
L114-280-5 In distribution
L129-518 In distribution
70-0828-1615 In distribution
70-0828-1515 In distribution
70-0828-1115 In distribution
L114-280-1 In distribution
L129-520 In distribution
180-103 In distribution
L129-515 In distribution
70-1228-0915 In distribution
L129-517 In distribution
70-1228-1115 In distribution
114-280-1 In distribution
70-0828-1415 In distribution
L129-521 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Peridot Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 10,850
Yellowstone Summit Spine 6,654
CoRoent Nuvasive, Inc. 5,690
Zavation Zavation 2,554
Anyplus II Spinal Fixation System GS Medical Co., Ltd. 2,533
Talos® IBF Meditech Spine, LLC 2,163
Peridot-PT Intervertebral body fusion system Gbs Commonwealth Co., Ltd. 1,956
TirboLOX-L Lumbar Ibfd Captiva Spine, Inc. 1,926
Endoskeleton® TL Titan Spine, LLC 1,896
Evos Lumbar Interbody System Cutting Edge Spine 1,871
Epiphany Pantheon Spinal LLC 1,507
LnK Lumbar Interbody Fusion Cage System L&K Biomed Co., Ltd. 1,506

Showing 12 of 1,958. All products under Intervertebral Fusion Device With Bone Graft, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K261430 2026-07-28
K260837 2026-05-12
K253748 2026-01-23
K251502 2025-07-07
K250373 2025-04-09
K243668 2025-01-23
K242826 2024-10-08
K232611 2023-11-30
K223430 2023-05-04
K221806 2022-12-05
K213417 2022-09-29
K212520 2021-10-08
K210061 2021-04-30
K203361 2021-03-17
K201721 2020-09-04
K201500 2020-08-04
K193521 2020-02-06
K193258 2020-01-31
K190721 2019-11-14
K190488 2019-07-23
K191005 2019-06-13
K181625 2018-12-11
K182470 2018-11-26
K172105 2018-02-02
K173182 2017-12-20
K170919 2017-08-03
K153400 2016-03-07
K133717 2014-09-19
K131077 2013-07-17
K130630 2013-06-13
K121116 2012-05-08
K111569 2011-07-06
K080411 2008-05-15

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P000028 2004-06-18 AFFINITY ANTERIOR CERVICAL CAGE SYSTEM Medtronic Sofamor Danek USA, Inc.
P970015 2003-09-10 LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE Sofamor Danek
P980048 2001-04-20 BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM Sulzer Spine-Tech
P950019 1999-03-19 RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION Stryker Spine
P950002 1997-06-30 BAK INTERBODY FUSION SYSTEM Zimmer Spine, Inc.

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer