Aries-TC

Aries-TC is a lumbar interbody fusion cage that maintains disc space distraction and structural stability while fusion develops. It is used in skeletally mature patients with degenerative…

Registry build 21.09.26

Aries-TC is a lumbar interbody fusion cage that maintains disc space distraction and structural stability while fusion develops. It is used in skeletally mature patients with degenerative disc disease at one or two contiguous levels from L2 to S1, including up to Grade 1 spondylolisthesis or retrolisthesis.

The implant is made from 3D printed titanium alloy. An axial opening holds bone graft, and protrusions on the upper and lower surfaces engage the adjacent vertebral endplates to resist expulsion. The range includes fixed heights and footprints for different anatomy and surgical approaches.

Listed Item

10x30x14, 0 Deg, Sterile, TLIF Interbody, Aries-TC

Treatment Requirements

Use requires autogenous bone graft and/or cancellous or corticocancellous allograft together with supplemental fixation. Patients should have received at least six months of nonoperative treatment. The implants are supplied sterile for single use.

14manufacturers in China registered for this device type
39catalogue numbers in this listing
1510(k) clearance

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 Aries-TC
Listed by Osseus Fusion Systems LLC, 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 Specification developer, Repacker / relabeller, Manufacturer
510(k) K181347
Record published 2021-12-22
Record revised 2025-07-14 (version 2)

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

Catalogue Numbers

Catalogue numbers for Aries-TC
Catalogue number Size Status
1200-0207 In distribution
1200-1205 In distribution
1200-1204 In distribution
1200-1701 In distribution
1200-0200 In distribution
1200-1206 In distribution
1200-0704 In distribution
1200-1207 In distribution
1200-0700 In distribution
1200-0204 In distribution
1200-0709 In distribution
1200-1200 In distribution
1200-0203 In distribution
1200-0706 In distribution
1200-0708 In distribution
1200-1205 In distribution
1200-1708 In distribution
1200-1702 In distribution
1200-0201 In distribution
12001705 In distribution
1200-1202 In distribution
1200-0208 In distribution
1200-0209 In distribution
1200-0202 In distribution
1200-1203 In distribution
1200-0702 In distribution
1200-1208 In distribution
1200-1707 In distribution
1200-1201 In distribution
1200-1703 In distribution
1200-1209 In distribution
1200-1700 In distribution
1200-1704 In distribution
1200-0206 In distribution
1200-0705 In distribution
1200-0703 In distribution
1200-1706 In distribution
1200-0707 In distribution
1200-1708 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
K181347 2018-08-15

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