Dyna-Link Ti

36 catalogue numbers from L125-799, listed by Life Spine, United States, under Intervertebral Fusion Device With Integrated Fixation, Lumbar. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
36catalogue numbers in this listing
4510(k) clearances naming this product code

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 Dyna-Link Ti
Listed by Life Spine, United States
FDA product code OVD
Device type Intervertebral Fusion Device With Integrated Fixation, Lumbar
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Manufacturer
510(k) K191834
Record published 2021-07-01
Record revised 2025-07-14 (version 2)

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

Catalogue Numbers

Catalogue numbers for Dyna-Link Ti
Catalogue number Size Status
L125-799 In distribution
83-003 In distribution
L114-881-3 In distribution
L125-797 In distribution
L125-683 In distribution
2020-0035 In distribution
L125-724 In distribution
L125-1032 In distribution
83-005 In distribution
L114-881-1 In distribution
L125-1002 In distribution
L114-881-5 In distribution
L125-672 In distribution
L125-1050 In distribution
83-3828-0613T In distribution
83-3828-1815T In distribution
L125-1022 In distribution
L125-1036 In distribution
L125-707 In distribution
L125-1004 In distribution
L125-1054 In distribution
83-001 In distribution
L125-723 In distribution
L125-697 In distribution
2020-0033 In distribution
L125-725 In distribution
83-3424-0611T In distribution
L125-1038 In distribution
L125-691 In distribution
83-004 In distribution
83-002 In distribution
125-726 In distribution
2020-0036 In distribution
L114-881-4 In distribution
L114-881-2 In distribution
L125-173 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
K200338 2020-04-17
K191834 2019-12-16
K180215 2018-09-13
K091301 2009-12-15

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