BluEX-TM Lumbar Interbody Fusion Cage System

BluEX-TM is an expandable lumbar interbody fusion cage used with bone graft and supplemental fixation. It is intended for skeletally mature patients with degenerative disc disease at one or…

Registry build 21.09.26

BluEX-TM is an expandable lumbar interbody fusion cage used with bone graft and supplemental fixation. It is intended for skeletally mature patients with degenerative disc disease at one or two adjacent levels from L2 to S1 after at least six months of nonoperative treatment.

The hollow rectangular titanium alloy implant is inserted in an unexpanded state and then increased in height using system instruments. Serrations on its upper and lower surfaces help secure it between the vertebral bodies. It is placed through a transforaminal or posterior approach.

Listed Item

BluEX-TM (25 X 11 X 11 mm, 15°)

Graft and Fixation

The cage is used with autogenous graft or allogeneic cancellous or corticocancellous bone graft. A supplemental fixation system is required. The indication permits up to Grade 1 spondylolisthesis or retrolisthesis at the treated level.

14manufacturers in China registered for this device type
36catalogue numbers in this listing
11510(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 BluEX-TM Lumbar Interbody Fusion Cage System
Listed by L&K Biomed Co., Ltd., South Korea
FDA product code MAX
Device type Intervertebral Fusion Device With Bone Graft, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer, Exporter
510(k) K251741
Record published 2026-04-15

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for BluEX-TM Lumbar Interbody Fusion Cage System
Catalogue number Size Status
JPT2511-0708S In distribution
JPT2511-0912S In distribution
JPT2211-0900S In distribution
JPT2511-0704S In distribution
JPT2211-0712S In distribution
JPT2211-0704S In distribution
JPT2511-0720S In distribution
JPT2511-1115S In distribution
JPT2511-0712S In distribution
JPT2211-0904S In distribution
JPT2211-0908S In distribution
JPT2511-0908S In distribution
JPT2211-0700S In distribution
JPT2511-1120S In distribution
JPT2511-0900S In distribution
JPT2511-1100S In distribution
JPT2511-0700S In distribution
JPT2211-1100S In distribution
JPT2211-0912S In distribution
JPT2511-1104S In distribution
JPT2211-0920S In distribution
JPT2211-0915S In distribution
JPT2511-0920S In distribution
JPT2211-1108S In distribution
JPT2511-0915S In distribution
JPT2211-1112S In distribution
JPT2211-1115S In distribution
JPT2511-0715S In distribution
JPT2211-1104S In distribution
JPT2511-1108S In distribution
JPT2511-0904S In distribution
JPT2211-0708S In distribution
JPT2511-1112S In distribution
JPT2211-1120S In distribution
JPT2211-0715S In distribution
JPT2211-0720S 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
K251741 2025-07-08
K242829 2024-10-23
K231680 2023-08-24
K223474 2023-01-13
K213441 2022-03-09
K190708 2019-09-16
K181380 2018-09-11
K151140 2015-08-18
K121096 2012-07-06
K120063 2012-04-19
K110783 2011-10-24

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