Idys®-ALIF ZP 3DTI

Alif Cage

Registry build 21.09.26
14manufacturers in China registered for this device type
60catalogue 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 Idys®-ALIF ZP 3DTI
Listed by Clariance, 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
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K192168
Record published 2020-01-23
Record revised 2025-07-14 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Sizes Height 12 to 18 mm; width 32 to 40 mm; depth 24 to 34 mm; angle 6 to 18 °

Catalogue Numbers

Catalogue numbers for Idys®-ALIF ZP 3DTI
Catalogue number Size Status
45572614-S Height 16 mm In distribution
45574810-S Height 18 mm In distribution
45573814-S Depth 30 mm In distribution
45573806-S Angle 6 ° In distribution
45574410-S Width 40 mm In distribution
45571814-S Height 18 mm In distribution
45572618-S Width 35 mm In distribution
45573418-S Depth 24 mm In distribution
45574818-S Height 18 mm In distribution
45574814-S Width 40 mm In distribution
45574614-S Height 16 mm In distribution
45571610-S Angle 10 ° In distribution
45572414-S Width 35 mm In distribution
45571418-S Depth 27 mm In distribution
45573818-S Angle 18 ° In distribution
45573810-S Angle 10 ° In distribution
45572206-S Depth 26 mm In distribution
45573214-S Angle 14 ° In distribution
45573614-S Width 40 mm In distribution
45574610-S Depth 34 mm In distribution
45571818-S Width 32 mm In distribution
45571806-S Depth 27 mm In distribution
45573414-S Height 14 mm In distribution
45572406-S Depth 30 mm In distribution
45573410-S Width 40 mm In distribution
45573610-S Angle 10 ° In distribution
45574206-S Depth 34 mm In distribution
45571614-S Angle 14 ° In distribution
45573406-S Width 40 mm In distribution
45571210-S Width 32 mm In distribution
45574210-S Depth 34 mm In distribution
45573206-S Height 12 mm In distribution
45572810-S Depth 30 mm In distribution
45571618-S Height 16 mm In distribution
45574414-S Height 14 mm In distribution
45573210-S Depth 30 mm In distribution
45572606-S Depth 30 mm In distribution
45571206-S Height 12 mm In distribution
45571410-S Width 32 mm In distribution
45572806-S Height 18 mm In distribution
45572210-S Height 12 mm In distribution
45571606-S Depth 27 mm In distribution
45574606-S Width 40 mm In distribution
45574618-S Height 16 mm In distribution
45572818-S Height 18 mm In distribution
45572814-S Angle 14 ° In distribution
45574214-S Width 40 mm In distribution
45572214-S Depth 30 mm In distribution
45574806-S Depth 34 mm In distribution
45571214-S Depth 27 mm In distribution
45572610-S Height 16 mm In distribution
45574406-S Angle 6 ° In distribution
45574418-S Angle 18 ° In distribution
45572410-S Width 35 mm In distribution
45571406-S Width 32 mm In distribution
45571810-S Angle 10 ° In distribution
45573606-S Height 16 mm In distribution
45572418-S Depth 30 mm In distribution
45571414-S Depth 27 mm In distribution
45573618-S Depth 30 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
K243670 2024-12-31
K200919 2021-04-12
K200920 2020-05-29
K183259 2019-03-01
K172465 2017-12-15
K131178 2013-10-10

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