Anyplus Peek Cage System

The GS Medical AnyPlus® PEEK Cage System device is designed for restoring the height of the intervertebral space after resection of the disc. AnyPlus® PEEK Cage System device consists of…

Registry build 21.09.26

The GS Medical AnyPlus® PEEK Cage System device is designed for restoring the height of the intervertebral space after resection of the disc. AnyPlus® PEEK Cage System device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The intervertebral body fusion devices are made of poly-ether-ether- ketone (PEEK Optima LT1) body with the X-ray (radio-opaque) markers made of Tantalum. The AnyPlus® PEEK Cage System devices are radiolucent allowing X-ray visualization to verify device placement. AnyPlus® PEEK Cage System device is supplied sterile and non-sterile and is intended for single use only. AnyPlus® PEEK Cage System is designed for interbody stabilization of the cervical spine.

14manufacturers in China registered for this device type
96catalogue numbers in this listing
4510(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 Anyplus Peek Cage System
Listed by GS Medical 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 Manufacturer
510(k) K200592
Record published 2026-04-22

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, manufacturing date

Catalogue Numbers

Catalogue numbers for Anyplus Peek Cage System
Catalogue number Size Status
1226-1010 In distribution
1192-5410 In distribution
1224-0005 In distribution
1192-5411 In distribution
1224-5012 In distribution
1190-1209 In distribution
1192-1408 In distribution
1225-1007 In distribution
1226-1011 In distribution
1224-0007 In distribution
1192-1409 In distribution
1223-5010 In distribution
1223-5009 In distribution
1223-0010 In distribution
1223-1010 In distribution
1223-5005 In distribution
1223-5007 In distribution
1223-0008 In distribution
1224-5006 In distribution
1224-5011 In distribution
1190-5211 In distribution
1224-1007 In distribution
1223-0011 In distribution
1224-5010 In distribution
1224-0012 In distribution
1224-1005 In distribution
1192-5409 In distribution
1192-5412 In distribution
1223-5011 In distribution
1223-1007 In distribution
1224-0009 In distribution
1226-1007 In distribution
1190-5210 In distribution
1192-5405 In distribution
1190-1212 In distribution
1190-5209 In distribution
1226-1005 In distribution
1224-5008 In distribution
1225-1012 In distribution
1223-5012 In distribution
1225-1005 In distribution
1226-1009 In distribution
1192-5407 In distribution
1192-5406 In distribution
1192-1410 In distribution
1224-1010 In distribution
1225-1006 In distribution
1225-1008 In distribution
1224-0011 In distribution
1192-1405 In distribution
1192-1411 In distribution
1224-1012 In distribution
1190-1210 In distribution
1190-5205 In distribution
1190-5208 In distribution
1224-0010 In distribution
1190-1206 In distribution
1226-1006 In distribution
1223-5008 In distribution
1223-1009 In distribution
1226-1008 In distribution
1223-0006 In distribution
1192-1412 In distribution
1225-1011 In distribution
1223-1012 In distribution
1190-5206 In distribution
1224-5009 In distribution
1190-1211 In distribution
1223-0012 In distribution
1224-1009 In distribution
1224-1011 In distribution
1190-5207 In distribution
1224-0008 In distribution
1224-1008 In distribution
1224-1006 In distribution
1225-1010 In distribution
1190-1208 In distribution
1190-5212 In distribution
1223-0009 In distribution
1192-1406 In distribution
1190-1205 In distribution
1192-1407 In distribution
1224-5007 In distribution
1190-1207 In distribution
1223-1006 In distribution
1226-1012 In distribution
1223-1011 In distribution
1223-0005 In distribution
1223-5006 In distribution
1223-1005 In distribution
1225-1009 In distribution
1224-5005 In distribution
1223-1008 In distribution
1223-0007 In distribution
1224-0006 In distribution
1192-5408 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
K223868 2023-04-26
K221687 2022-07-27
K131612 2014-04-18
K111354 2011-10-17

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