NuVasive

CoRoent XL-W Trial Wndw, 60-16mm 10°Lord

Registry build 21.09.26
14manufacturers in China registered for this device type
119catalogue numbers in this listing
5510(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 NuVasive
Listed by Nuvasive, 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 Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K170962
Record published 2018-09-17
Record revised 2025-06-11 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for NuVasive
Catalogue number Size Status
6910512 In distribution
Z500116-112 In distribution
Z300033-208 In distribution
Z200154-08 In distribution
Z200221-116 In distribution
Z200173 In distribution
Z200069-012 In distribution
Z200069-114 In distribution
Z500116-110 In distribution
Z500112-09 In distribution
Z300102-16 In distribution
Z500112-07 In distribution
Z300120 In distribution
Z500511 In distribution
Z200181-100 In distribution
6901510 In distribution
6961250 In distribution
Z200069-014 In distribution
Z200041-116 In distribution
Z300079-16 In distribution
Z200175-14 In distribution
Z200170-212 In distribution
Z300130-306 In distribution
Z200170-208 In distribution
Z200154-12 In distribution
Z500116-212 In distribution
Z200041-008 In distribution
Z300130-310 In distribution
Z200071-1 In distribution
Z200069-116 In distribution
Z300079-216 In distribution
Z200041-114 In distribution
Z500113-12 In distribution
6961050 In distribution
Z300079-416 In distribution
6950850 In distribution
Z300102-10 In distribution
Z300045-504 In distribution
Z300102-14 In distribution
Z300030-110 In distribution
Z200221-016 In distribution
Z200225-10 In distribution
Z500096-20 In distribution
6901608 In distribution
Z300079-314 In distribution
Z500112-11 In distribution
5450027 In distribution
Z200221-012 In distribution
Z300079-414 In distribution
Z200041-010 In distribution
Z300030-106 In distribution
Z500116-214 In distribution
Z500112-10 In distribution
Z200069-008 In distribution
Z300007-516 In distribution
Z200222-116 In distribution
Z200211 In distribution
6901508 In distribution
Z300045-02 In distribution
Z200154-10 In distribution
Z500100-06 In distribution
5450040 In distribution
6910510 In distribution
Z500116-108 In distribution
Z200175-08 In distribution
Z300130-206 In distribution
6910612 In distribution
Z300130-406 In distribution
Z200026-02 In distribution
Z300018-500 In distribution
Z300033-106 In distribution
Z400001 In distribution
Z300007-520 In distribution
Z300102-12 In distribution
Z300045-04 In distribution
Z200069-110 In distribution
Z300140 In distribution
Z300079-312 In distribution
6901512 In distribution
Z200222-014 In distribution
Z200181-200 In distribution
Z200221-014 In distribution
Z200222-008 In distribution
Z200222-016 In distribution
Z200164 In distribution
Z500117-01 In distribution
Z500113-07 In distribution
Z300130-410 In distribution
6901610 In distribution
Z300007-512 In distribution
Z200181 In distribution
Z200221-108 In distribution
Z200044-08 In distribution
Z200217 In distribution
Z300130-110 In distribution
Z500113-13 In distribution
6904485 In distribution
Z400057-30 In distribution
6900101 In distribution
Z200041-012 In distribution
Z400077 In distribution
Z200222-110 In distribution
Z300007-510 In distribution
6961450 In distribution
Z300007-518 In distribution
Z300045-01 In distribution
Z300098-01 In distribution
Z500133 In distribution
Z200178-1 In distribution
Z300030-108 In distribution
Z200041-110 In distribution
Z200222-010 In distribution
Z300023 In distribution
Z200069-112 In distribution
Z300079-10 In distribution
Z300033-210 In distribution
Z200221-212 In distribution
Z200178-2 In distribution
Z200221-114 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
K141665 2015-03-13
K140319 2014-10-09
K140162 2014-07-02
K120918 2012-06-28
K071795 2007-12-04

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