Pro-Link Ti

67 catalogue numbers from 129-451, listed by Life Spine, United States, under Intervertebral Fusion Device With Integrated Fixation, Cervical. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
67catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (2), Guangdong (1), Jiangsu (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OVE
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10

Record

Regulatory record for Pro-Link Ti
Listed by Life Spine, United States
FDA product code OVE
Device type Intervertebral Fusion Device With Integrated Fixation, Cervical
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Manufacturer
510(k) K160066
Record published 2019-11-07
Record revised 2025-07-14 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Pro-Link Ti
Catalogue number Size Status
129-451 In distribution
23-1411-710T In distribution
129-468 In distribution
113-1016 In distribution
113-1019 In distribution
113-1712 In distribution
113-1721 In distribution
113-1011 In distribution
113-1020 In distribution
113-1718 In distribution
113-1012 In distribution
114-103-5 In distribution
113-1709 In distribution
113-1008 In distribution
20-1411-707T In distribution
113-1705 In distribution
23-1411-709T In distribution
113-1708 In distribution
129-361 In distribution
113-1021 In distribution
113-1720 In distribution
113-886 In distribution
113-1007 In distribution
129-445 In distribution
113-1711 In distribution
113-885 In distribution
114-103-2 In distribution
113-1005 In distribution
129-390 In distribution
113-741 In distribution
113-1010 In distribution
113-1715 In distribution
23-1411-711T In distribution
113-1722 In distribution
113-1015 In distribution
114-103-3 In distribution
113-1009 In distribution
113-887 In distribution
113-1022 In distribution
113-882 In distribution
129-362 In distribution
113-1006 In distribution
20-1411-706T In distribution
129-376 In distribution
129-460 In distribution
113-1017 In distribution
113-1717 In distribution
113-1716 In distribution
20-1411-705T In distribution
129-393 In distribution
113-1707 In distribution
113-880 In distribution
129-360 In distribution
129-458 In distribution
113-1710 In distribution
129-351 In distribution
113-1706 In distribution
113-884 In distribution
113-1719 In distribution
129-379 In distribution
129-377 In distribution
113-883 In distribution
113-1018 In distribution
129-471 In distribution
23-1411-712T In distribution
113-881 In distribution
20-1411-708T In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
IdentiTi Alphatec Spine, Inc. 630
Dolomite Astura Medical 607
CoRoent Nuvasive, Inc. 580
Aeon-C Diomedical Co., Ltd. 508
Tomcat™ Cervical Spinal System Choice Spine, LP 468
Shoreline ACS Seaspine Orthopedics Corporation 428
Zavation Zavation 423
Alta™ Stand-Alone Interbody Fusion System Biomet Spine 404
Unison™-C Anterior Cervical Fixation System Pioneer Surgical Technology, Inc. 334
Chesapeake® Stabilization System VB Spine LLC 272
UniSpace® Stand-Alone C Cage CG MedTech Co., Ltd. 260
Solitaire-C Cervical Spacer Biomet Spine 256

Showing 12 of 391. All products under Intervertebral Fusion Device With Integrated Fixation, Cervical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K231704 2023-10-19
K180642 2018-05-10
K160066 2016-09-02
K121151 2012-11-16

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