Reliance Cervical IBF System

Cervical IBF-HA PEEK-STERILE, 14mm x 11mm x 10mm, 0°, PEEK OPTIMA LT1-HA

Registry build 21.09.26
7manufacturers in China registered for this device type
26catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

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

Chinese manufacturers registered for FDA product code ODP
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
Zhisu Health Tech Jiaxing Co., Ltd. Tongxiang Zhejiang Contract manufacturer 4
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Zhejiang Decans Medical Devices Co., Ltd. Jiaxing Zhejiang Manufacturer 10
Shanghai Sanyou Medical Co., Ltd. Shanghai Shanghai Manufacturer 6

Record

Regulatory record for Reliance Cervical IBF System
Listed by VY Spine, LLC, United States
FDA product code ODP
Device type Intervertebral Fusion Device With Bone Graft, Cervical
Device class Class 2
Regulation 21 CFR 888.3080
Establishment Specification developer, Manufacturer
Record published 2016-12-09
Record revised 2026-03-03 (version 5)

Specifications

Specifications
MRI safety MR Unsafe
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Distribution end date 2026-03-02

Catalogue Numbers

Catalogue numbers for Reliance Cervical IBF System
Catalogue number Size Status
1-01-005 In distribution
1-02-008-HAG In distribution
1-02-707-HAG In distribution
1-02-705HA In distribution
1-02-708-HAG In distribution
1-02-006HA In distribution
1-02-709-HAG In distribution
1-02-007-HAG In distribution
1-01-011 In distribution
1-03-705 In distribution
1-01-009 In distribution
1-02-705-HAG In distribution
1-03-707 In distribution
1-01-704 In distribution
1-01-710 In distribution
1-01-007 In distribution
1-01-706 In distribution
1-03-709 In distribution
1-02-006-HAG In distribution
1-02-010-HAG In distribution
1-02-004HA In distribution
1-02-707HA In distribution
1-01-708 In distribution
1-02-704-HAG In distribution
1-03-711 In distribution
1-02-008HA Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Latitude-C AM™ Cervical Interbody Fusion System Degen Medical 1,529
IdentiTi Alphatec Spine, Inc. 1,390
Zavation Zavation 1,357
IVA Cage Ti Diomedical Co., Ltd. 1,202
Latitude-C Cervical Interbody Spacer System Degen Medical 1,185
Peridot Anterior Cervical Intervertebral Body Fusion System Gbs Commonwealth Co., Ltd. 1,056
Aleutian® Interbody Systems VB Spine LLC 1,017
Valeo Spacer System Sintx Technologies Inc. 918
Cascadia™ Interbody System VB Spine LLC 823
CoRoent Nuvasive, Inc. 815
Tyber Medical Tyber Medical 740
Matisse Anterior Cervical Interbody Fusion Cage System CTL Medical Corporation 577

Showing 12 of 938. All products under Intervertebral Fusion Device With Bone Graft, Cervical

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K231836 2023-10-30
K230414 2023-05-12
K223513 2023-04-18
K221162 2022-11-04
K212715 2021-12-20

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