NuVasive

CoRoent XL-W Trial, 10x60mm 15° Lordotic

Registry build 21.09.26
1manufacturer
55catalogue numbers in this listing

Who Else Makes It

Registered in Shandong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code PHM
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42

Record

Regulatory record for NuVasive
Listed by Nuvasive, Inc., United States
FDA product code PHM
Device type Intervertebral Fusion Device With Bone Graft, Thoracic
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K170962
Record published 2019-08-30
Record revised 2025-06-11 (version 8)

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, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for NuVasive
Catalogue number Size Status
Z200041-210 In distribution
Z500100-10 In distribution
6910610 In distribution
6910508 In distribution
Z500096-26 In distribution
Z500112-13 In distribution
Z500113-14 In distribution
Z200175-12 In distribution
Z500113-09 In distribution
Z200221-008 In distribution
Z200189 In distribution
Z500112-12 In distribution
6910614 In distribution
Z200069-010 In distribution
Z500112-14 In distribution
Z200069-108 In distribution
Z500113-08 In distribution
Z200222-108 In distribution
Z200071-2 In distribution
Z200041-212 In distribution
Z200175-10 In distribution
Z400065-25 In distribution
Z200069-016 In distribution
Z200221-010 In distribution
6901612 In distribution
Z200222-114 In distribution
Z200041-016 In distribution
Z500111 In distribution
Z500112-08 In distribution
Z500117-02 In distribution
Z200170-112 In distribution
Z200222-012 In distribution
Z500116-210 In distribution
Z200185 In distribution
Z200170-210 In distribution
Z200221-110 In distribution
Z200221-208 In distribution
Z300018 In distribution
Z200222-112 In distribution
Z500100-08 In distribution
Z200221-210 In distribution
Z200041-112 In distribution
6910608 In distribution
Z200221-112 In distribution
Z500113-10 In distribution
Z200026-01 In distribution
Z200170-110 In distribution
Z500113-11 In distribution
Z200041-108 In distribution
Z500116-114 In distribution
Z200179-08 In distribution
Z200041-208 In distribution
Z200170-108 In distribution
Z200041-014 In distribution
Z700163 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CoRoent Nuvasive, Inc. 2,299
IdentiTi Alphatec Spine, Inc. 940
Solar™ Interbody Fusion System Degen Medical 805
Transcend Nanotec Alphatec Spine, Inc. 466
IDENTITi Nanotec Alphatec Spine, Inc. 459
E3D-A Interbody System Evolution Spine, LLC 308
Battalion Alphatec Spine, Inc. 241
Reef L Seaspine Orthopedics Corporation 207
IdentiTi II Alphatec Spine, Inc. 163
Modulus Nuvasive, Inc. 158
Hedron Globus Medical, Inc. 156
Roccia Silony Medical Gmbh 133

Showing 12 of 41. All products under Intervertebral Fusion Device With Bone Graft, Thoracic

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