Px™

119 catalogue numbers from X21014220, listed by Inno-Health Technology Co., Ltd., Taiwan, under Intervertebral Fusion Device With Bone Graft, Lumbar. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
119catalogue numbers in this listing

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 Px™
Listed by Inno-Health Technology Co., Ltd., Taiwan
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, Contract steriliser, Manufacturer
Record published 2015-07-16
Record revised 2026-01-08 (version 9)

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, serial number
Sizes Angle 0 to 5 °; length 22 to 32 mm; height 8 to 16 mm; width 8 to 12 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Px™
Catalogue number Size Status
X21014220 Angle 0 ° In distribution
X21011220 Width 10 mm In distribution
X21012220 Width 10 mm In distribution
X20812250 Width 8 mm In distribution
X20815250 Width 8 mm In distribution
LS-240 In distribution
X21011250 Width 10 mm In distribution
X20811225 Width 8 mm In distribution
X21209300 Angle 0 ° In distribution
X20816255 Width 8 mm In distribution
X20811255 Width 8 mm In distribution
X21013280 Angle 0 ° In distribution
X21010320 Width 10 mm In distribution
X20810225 Width 8 mm In distribution
X20809250 Angle 0 ° In distribution
X20808220 Angle 0 ° In distribution
X21008225 Width 10 mm In distribution
X21008320 Width 10 mm In distribution
X21015255 Angle 5 ° In distribution
X21009250 Width 10 mm In distribution
X21012280 Width 10 mm In distribution
X20812220 Width 8 mm In distribution
X21210320 Angle 0 ° In distribution
X20813225 Width 8 mm In distribution
X21208280 Angle 0 ° In distribution
X21015225 Angle 5 ° In distribution
LS-181 In distribution
X21014255 Angle 5 ° In distribution
X21212300 Angle 0 ° In distribution
X21010225 Width 10 mm In distribution
X20813220 Width 8 mm In distribution
X21014250 Angle 0 ° In distribution
X21010250 Width 10 mm In distribution
X21011225 Width 10 mm In distribution
X21009255 Width 10 mm In distribution
X21008250 Width 10 mm In distribution
X20811250 Width 8 mm In distribution
X21210300 Angle 0 ° In distribution
X20816225 Width 8 mm In distribution
X21015280 Angle 0 ° In distribution
X21016225 Angle 5 ° In distribution
X20812255 Width 8 mm In distribution
X20812225 Width 8 mm In distribution
X20808255 Angle 5 ° In distribution
X21215300 Angle 0 ° In distribution
X21008220 Width 10 mm In distribution
X20808250 Angle 0 ° In distribution
X21013225 Width 10 mm In distribution
X21016255 Angle 5 ° In distribution
X21216300 Angle 0 ° In distribution
X20816250 Width 8 mm In distribution
X20814220 Width 8 mm In distribution
X20816220 Width 8 mm In distribution
X20815225 Width 8 mm In distribution
X21012320 Width 10 mm In distribution
X21013250 Width 10 mm In distribution
X21215280 Angle 0 ° In distribution
X20815255 Width 8 mm In distribution
X21011320 Width 10 mm In distribution
LS-263 In distribution
LS-211 In distribution
X21214280 Angle 0 ° In distribution
X21016220 Angle 0 ° In distribution
X21211280 Angle 0 ° In distribution
X20814250 Width 8 mm In distribution
X20809225 Angle 5 ° In distribution
X21011280 Width 10 mm In distribution
X21209320 Angle 0 ° In distribution
X21015220 Angle 0 ° In distribution
X20809255 Angle 5 ° In distribution
X20810250 Width 8 mm In distribution
X21008280 Width 10 mm In distribution
X21010255 Width 10 mm In distribution
X21216280 Angle 0 ° In distribution
X21009280 Width 10 mm In distribution
X20814225 Width 8 mm In distribution
X21213320 Angle 0 ° In distribution
X20814255 Width 8 mm In distribution
X21014320 Angle 0 ° In distribution
X20813255 Width 8 mm In distribution
X21015250 Angle 0 ° In distribution
X21210280 Angle 0 ° In distribution
X20810220 Width 8 mm In distribution
X21013220 Width 10 mm In distribution
X21211320 Angle 0 ° In distribution
X21016250 Angle 0 ° In distribution
X21009320 Width 10 mm In distribution
X21010280 Width 10 mm In distribution
X21214320 Angle 0 ° In distribution
X20809220 Angle 0 ° In distribution
X21009225 Width 10 mm In distribution
X21213300 Angle 0 ° In distribution
X21211300 Angle 0 ° In distribution
X21014225 Angle 5 ° In distribution
X20808225 Width 8 mm In distribution
X21216320 Angle 0 ° In distribution
X21014280 Angle 0 ° In distribution
X21009220 Width 10 mm In distribution
X20815220 Width 8 mm In distribution
X21012255 Width 10 mm In distribution
LS-258 In distribution
X21013320 Angle 0 ° In distribution
X20811220 Width 8 mm In distribution
X21213280 Angle 0 ° In distribution
X21212320 Angle 0 ° In distribution
X21015320 Angle 0 ° In distribution
X20810255 Width 8 mm In distribution
X21013255 Width 10 mm In distribution
X21012225 Width 10 mm In distribution
X21008255 Width 10 mm In distribution
X21011255 Width 10 mm In distribution
X21214300 Angle 0 ° In distribution
LS-241 In distribution
X21010220 Width 10 mm In distribution
X21212280 Angle 0 ° In distribution
X20813250 Width 8 mm In distribution
X21209280 Angle 0 ° In distribution
X21012250 Width 10 mm In distribution
X21215320 Angle 0 ° 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

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