Nest Interbody System

NEST is a hollow rectangular lumbar interbody cage combining solid and porous titanium-alloy structures. It supports the space between vertebrae during interbody fusion, with serrations on…

Registry build 21.09.26

NEST is a hollow rectangular lumbar interbody cage combining solid and porous titanium-alloy structures. It supports the space between vertebrae during interbody fusion, with serrations on the porous upper and lower surfaces.

Graft windows hold autogenous or allogeneic bone within the cage. The implant is additively manufactured from Ti-6Al-4V alloy and offered in different dimensions and lordotic angles.

Supply and Fixation

The cages are supplied sterile and require supplemental lumbosacral fixation. Their lumbar fusion indication covers one or two adjacent levels from L2 to S1 in skeletally mature patients, using cancellous and/or corticocancellous graft.

14manufacturers in China registered for this device type
23catalogue numbers in this listing
2510(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 Nest Interbody System
Listed by Paonan Biotech 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 Manufacturer
510(k) K180230
Record published 2026-05-04

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
Sizes Width 8 to 9 mm; length 26 to 30 mm; height 8 to 14 mm; angle 12 °

Catalogue Numbers

Catalogue numbers for Nest Interbody System
Catalogue number Size Status
21001009261104 Width 9 mm In distribution
21001009281404 Width 9 mm In distribution
21001009280904 Width 9 mm In distribution
21001009301204 Width 9 mm In distribution
21001009261204 Width 9 mm In distribution
21001009281104 Width 9 mm In distribution
21001009261004 Width 9 mm In distribution
21001009260904 Width 9 mm In distribution
21001009281304 Width 9 mm In distribution
21001009301004 Width 9 mm In distribution
21001009301104 Width 9 mm In distribution
21001009261304 Width 9 mm In distribution
21001009280803 Width 9 mm In distribution
21001009300803 Width 9 mm In distribution
21001009281204 Width 9 mm In distribution
21001008260803 Width 8 mm In distribution
21001009300904 Width 9 mm In distribution
21001009261404 Width 9 mm In distribution
21001008261404 Width 8 mm In distribution
21001009281004 Width 9 mm In distribution
21001009260803 Width 9 mm In distribution
21001009301404 Width 9 mm In distribution
21001009301304 Width 9 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
K180230 2019-01-25
K180228 2019-01-11

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