T-Lift®

Square Connect Driver Shaft, T-Lift, 14 DEG

Registry build 21.09.26
14manufacturers in China registered for this device type
142catalogue numbers in this listing
6510(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 T-Lift®
Listed by Spinefrontier, Inc., United States
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
510(k) K111553
Record published 2016-04-15
Record revised 2020-02-24 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Length 25 to 35 mm; height 6 to 17 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for T-Lift®
Catalogue number Size Status
01-05001-13 Length 25 mm In distribution
01-05005-12 Height 12 mm In distribution
11-05041-06 In distribution
01-05005-09 Length 35 mm In distribution
SI02862-07 In distribution
SI02862-04 In distribution
11-05042-07 In distribution
IM2014 Height 15 mm In distribution
01-05006-09 Height 9 mm In distribution
SI02862-09 In distribution
11-05042-11 In distribution
01-05006-07 Length 35 mm In distribution
IM2028 Length 25 mm In distribution
13-05002 In distribution
SI02862-03 In distribution
IM2033-03 Height 9 mm In distribution
SI02861-09 In distribution
01-05000-08 Length 25 mm In distribution
14-05006 In distribution
01-05003-13 Height 13 mm In distribution
01-05005-15 Height 15 mm In distribution
01-05005-13 Length 35 mm In distribution
SI02861-07 In distribution
IM2019 Length 25 mm In distribution
11-05041-08 In distribution
IM2031 Length 25 mm In distribution
IM2009 Length 25 mm In distribution
IM2016 Height 7 mm In distribution
01-05004-14 Height 14 mm In distribution
01-05004-15 Length 30 mm In distribution
11-05041-15 In distribution
11-05042-14 In distribution
SI02861-04 In distribution
IM2023 Height 10 mm In distribution
IM2001 Length 25 mm In distribution
14-05002 In distribution
01-05001-10 Length 25 mm In distribution
01-05004-12 Height 12 mm In distribution
01-05000-09 Height 9 mm In distribution
01-05001-14 Length 25 mm In distribution
01-05005-08 Length 35 mm In distribution
01-05001-08 Length 25 mm In distribution
SI02862-02 In distribution
01-05006-08 Length 35 mm In distribution
11-05042-09 In distribution
IM2006 Height 15 mm In distribution
SI02862-08 In distribution
14-05008 In distribution
01-05006-13 Length 35 mm In distribution
IM2022 Height 8 mm In distribution
01-05000-11 Length 25 mm In distribution
SI02861-02 In distribution
01-05000-12 Height 12 mm In distribution
11-05042-13 In distribution
01-05005-10 Length 35 mm In distribution
IM2029 Length 25 mm In distribution
14-05005 In distribution
11-05041-09 In distribution
11-05042-15 In distribution
SI02861-10 In distribution
11-05041-11 In distribution
IM2025 Height 14 mm In distribution
11-05042-10 In distribution
IM2030 Height 14 mm In distribution
01-05006-15 Height 15 mm In distribution
IM2011 Height 9 mm In distribution
01-05003-15 Height 15 mm In distribution
11-05042-12 In distribution
01-05001-15 Height 15 mm In distribution
IM2032-03 Length 25 mm In distribution
01-05001-12 Length 25 mm In distribution
SI02862-05 In distribution
01-05003-09 Length 30 mm In distribution
01-05004-09 Length 30 mm In distribution
IM2033-05 Height 11 mm In distribution
01-05004-08 Height 8 mm In distribution
01-05000-06 Height 6 mm In distribution
11-05041-12 In distribution
IM2015 Length 25 mm In distribution
01-05005-07 Length 35 mm In distribution
01-05005-11 Length 35 mm In distribution
01-05005-14 Height 14 mm In distribution
01-05004-11 Length 30 mm In distribution
SI02861-05 In distribution
01-05003-14 Height 14 mm In distribution
11-05042-06 In distribution
IM2005 Height 13 mm In distribution
14-05003 In distribution
SI02861-01 In distribution
IM2007 Length 25 mm In distribution
IM2013 Length 25 mm In distribution
01-05003-10 Height 10 mm In distribution
IM2012 Height 11 mm In distribution
IM2021 Length 25 mm In distribution
11-05041-13 In distribution
IM2024 Height 12 mm In distribution
01-05006-14 Height 14 mm In distribution
01-05003-06 Length 30 mm In distribution
IM2010 Height 7 mm In distribution
01-05001-07 Length 25 mm In distribution
11-05042-08 In distribution
SI02861-03 In distribution
SI02861-06 In distribution
IM2004 Height 13 mm In distribution
SI02862-01 In distribution
01-05003-08 Length 30 mm In distribution
11-05000 In distribution
01-05003-11 Height 11 mm In distribution
IM2002 Length 25 mm In distribution
14-05001 In distribution
SI02861-08 In distribution
SI02862-06 In distribution
01-05001-09 Height 9 mm In distribution
01-05001-11 Length 25 mm In distribution
11-05041-07 In distribution
14-05004 In distribution
01-05004-07 Length 30 mm In distribution
01-05006-10 Height 10 mm In distribution
01-05000-14 Length 25 mm In distribution
14-05009 In distribution
01-05000-15 Length 25 mm In distribution
01-05006-12 Height 12 mm In distribution
11-05041-14 In distribution
01-05004-13 Height 13 mm In distribution
01-05003-12 Length 30 mm In distribution
IM2027 Height 8 mm In distribution
14-05000 In distribution
01-05000-07 Length 25 mm In distribution
IM2003 Length 25 mm In distribution
IM2017 Height 9 mm In distribution
01-05003-07 Height 7 mm In distribution
01-05000-10 Length 25 mm In distribution
11-05041-10 In distribution
IM2020 Height 15 mm In distribution
01-05004-10 Height 10 mm In distribution
IM2008 Length 25 mm In distribution
14-05007 In distribution
01-05000-13 Height 13 mm In distribution
IM2032-05 Length 25 mm In distribution
IM2018 Height 11 mm In distribution
01-05005-06 Length 35 mm In distribution
01-05006-11 Height 11 mm 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
K193106 2020-06-19
K142504 2015-05-13
K111553 2011-09-28
K092815 2010-06-30
K091638 2009-09-14
K072289 2007-11-01

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