Pyxis 3d Titanium Cervical Cage, Close

173 catalogue numbers from 8062-1214S, listed by GS Medical Co., Ltd., South Korea, 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
173catalogue 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 Pyxis 3D Titanium Cervical Cage, Close
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) K241738
Record published 2026-01-28
Record revised 2026-05-15 (version 2)

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 Pyxis 3D Titanium Cervical Cage, Close
Catalogue number Size Status
8062-1214S In distribution
8071-0814S In distribution
8070-0812S In distribution
8070-0811S In distribution
0905-7525 In distribution
8060-0812S In distribution
0905-7555 In distribution
8070-1613S In distribution
8062-0812S In distribution
8062-1213S In distribution
0905-7585 In distribution
8062-0411S In distribution
8071-1611S In distribution
0905-7540 In distribution
8062-1211S In distribution
8071-1213S In distribution
0905-5550 In distribution
8072-1612S In distribution
8060-1614S In distribution
0905-5545 In distribution
8060-1214S In distribution
8071-0413S In distribution
8060-0814S In distribution
8061-1212S In distribution
0905-6565 In distribution
8061-1211S In distribution
0902-4555 In distribution
0905-6550 In distribution
8061-1612S In distribution
8062-1613S In distribution
8071-0011S In distribution
8060-0011S In distribution
8062-1614S In distribution
8070-0011S In distribution
8071-0012S In distribution
8070-0413S In distribution
8061-0013S In distribution
8071-1212S In distribution
8070-1612S In distribution
8070-0013S In distribution
8060-0813S In distribution
8061-1611S In distribution
8071-0014S In distribution
8072-0014S In distribution
8060-1213S In distribution
8061-0413S In distribution
8062-1611S In distribution
0902-4560 In distribution
0902-4545 In distribution
8061-1213S In distribution
0905-7580 In distribution
8071-0811S In distribution
8072-0012S In distribution
8072-0814S In distribution
8070-0012S In distribution
8070-1212S In distribution
0905-7595 In distribution
0905-5560 In distribution
8071-1613S In distribution
8072-0812S In distribution
0905-6585 In distribution
8061-1214S In distribution
8061-0811S In distribution
8060-0411S In distribution
8062-1212S In distribution
0905-7535 In distribution
8062-0014S In distribution
8062-0414S In distribution
8061-0411S In distribution
8071-0411S In distribution
8061-1613S In distribution
8061-0014S In distribution
8070-0813S In distribution
8061-0012S In distribution
0905-7575 In distribution
0902-4570 In distribution
8072-1211S In distribution
8070-1614S In distribution
8072-1213S In distribution
0905-5565 In distribution
8070-0014S In distribution
8062-0013S In distribution
8070-0411S In distribution
8060-0414S In distribution
8061-0813S In distribution
0902-4535 In distribution
0905-7570 In distribution
8071-1214S In distribution
8060-0413S In distribution
8072-0013S In distribution
0905-6540 In distribution
0905-7530 In distribution
0905-6545 In distribution
0902-4525 In distribution
8061-0812S In distribution
8070-1211S In distribution
0905-6535 In distribution
0902-4550 In distribution
8060-0412S In distribution
0905-5555 In distribution
8071-0813S In distribution
0905-6595 In distribution
8070-0814S In distribution
8062-0412S In distribution
8060-0811S In distribution
8071-1612S In distribution
8060-1212S In distribution
0905-5530 In distribution
0905-7500 In distribution
0905-6570 In distribution
8062-0811S In distribution
0905-7590 In distribution
8061-0814S In distribution
0902-4565 In distribution
8072-0411S In distribution
8060-1613S In distribution
8061-1614S In distribution
0905-5535 In distribution
0905-7565 In distribution
0905-7545 In distribution
8062-0413S In distribution
8070-1214S In distribution
0905-5525 In distribution
8061-0011S In distribution
0905-5540 In distribution
0905-7550 In distribution
8072-0011S In distribution
0905-6530 In distribution
8062-0813S In distribution
8072-1614S In distribution
8060-0013S In distribution
8070-0412S In distribution
8060-0014S In distribution
8072-0414S In distribution
8072-1214S In distribution
8071-0412S In distribution
0905-6500 In distribution
0905-6555 In distribution
8061-0412S In distribution
8060-1612S In distribution
8071-0414S In distribution
8071-0812S In distribution
8072-0813S In distribution
8060-1611S In distribution
8062-0012S In distribution
8072-0811S In distribution
8071-1614S In distribution
8071-1211S In distribution
GSVP-4000 In distribution
8072-1611S In distribution
0905-6575 In distribution
0905-7560 In distribution
8060-1211S In distribution
8062-0011S In distribution
0905-6580 In distribution
8071-0013S In distribution
8070-1611S In distribution
0902-4530 In distribution
0905-6525 In distribution
8061-0414S In distribution
8072-1212S In distribution
0905-5570 In distribution
8060-0012S In distribution
8070-1213S In distribution
8072-1613S In distribution
0902-4540 In distribution
8072-0413S In distribution
0905-6590 In distribution
8070-0414S In distribution
8062-1612S In distribution
0905-6560 In distribution
8062-0814S In distribution
8072-0412S 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