CoreLink Foundation 3d Lateral Cage

Foundation 3D Lateral Cage - 18mm x 45mm x 10mm, 12°

Registry build 21.09.26
3manufacturers in China registered for this device type
68catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Shandong (2), Jiangsu (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OVD
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for CoreLink Foundation 3D Lateral Cage
Listed by Corelink, LLC, United States
FDA product code OVD
Device type Intervertebral Fusion Device With Integrated Fixation, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
510(k) K231743
Record published 2025-01-06
Record revised 2025-11-20 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Radiation Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for CoreLink Foundation 3D Lateral Cage
Catalogue number Size Status
3LL1850-0810 In distribution
3LL2250-0014 In distribution
3LL1860-0808 In distribution
3LL2250-0012 In distribution
3LL1850-0808 In distribution
3LL1860-0812 In distribution
3LL1855-0808 In distribution
3LL2250-0810 In distribution
3LL2245-0812 In distribution
3LL2255-0812 In distribution
3LL2255-3020 In distribution
3LL2250-0808 In distribution
3LL1845-1210 In distribution
3LL2250-0812 In distribution
3LL1860-1210 In distribution
3LL2245-0814 In distribution
3LL2245-1212 In distribution
3LL2250-0008 In distribution
3LL1860-0810 In distribution
3LL2255-1212 In distribution
3LL2260-3018 In distribution
3LL1850-0814 In distribution
3LL1845-1214 In distribution
3LL1845-0810 In distribution
3LL2255-0810 In distribution
3LL1850-1214 In distribution
3LL1860-0814 In distribution
3LL2260-1210 In distribution
3LL2245-0012 In distribution
3LL1855-0810 In distribution
3LL2260-0810 In distribution
3LL2245-0010 In distribution
3LL2255-3018 In distribution
3LL1855-0814 In distribution
3LL2255-1210 In distribution
3LL1845-0808 In distribution
3LL2245-1210 In distribution
3LL2245-0808 In distribution
3LL2245-1214 In distribution
3LL2255-0808 In distribution
3LL2255-1214 In distribution
3LL2260-3016 In distribution
3LL2255-0814 In distribution
3LL1845-0812 In distribution
3LL2250-0814 In distribution
3LL1850-1210 In distribution
3LL2260-1214 In distribution
3LL2260-3020 In distribution
3LL2260-1212 In distribution
3LL1850-1212 In distribution
3LL2245-0008 In distribution
3LL1845-1212 In distribution
3LL2250-1212 In distribution
3LL2260-0814 In distribution
3LL1855-1214 In distribution
3LL1860-1214 In distribution
3LL1860-1212 In distribution
3LL2260-0808 In distribution
3LL2250-0010 In distribution
3LL1855-1212 In distribution
3LL1855-1210 In distribution
3LL1845-0814 In distribution
3LL1855-0812 In distribution
3LL2250-1210 In distribution
3LL2245-0810 In distribution
3LL2250-1214 In distribution
3LL2260-0812 In distribution
3LL1850-0812 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sirion Astura Medical 1,465
IdentiTi Alphatec Spine, Inc. 1,372
EL Capitan Astura Medical 1,205
Zavation Zavation 1,157
Brigade Nuvasive, Inc. 1,005
Solar™ Interbody Fusion System Degen Medical 899
Zavation F3D Corpectomy Zavation 730
ROI-A Ldr Spine USA 552
Avenue L Ldr Spine USA 524
Transcend Nanotec Alphatec Spine, Inc. 485
Endoskeleton® TL Hyperlordotic nanoLOCK® Surface Technology Titan Spine, LLC 462
Base Nuvasive, Inc. 462

Showing 12 of 241. All products under Intervertebral Fusion Device With Integrated Fixation, Lumbar

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K180814 2018-08-10

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