Dominion

Variable Lordosis Fixated Zero Endplate

Registry build 21.09.26
7manufacturers in China registered for this device type
36catalogue numbers in this listing
2510(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 Dominion
Listed by Astura Medical, 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, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2024-10-22
Record revised 2025-12-10 (version 4)

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
Sizes Outer diameter 12 to 15 mm; height 12 to 93 mm; depth 14 to 18 mm; length 12 to 18 mm

Catalogue Numbers

Catalogue numbers for Dominion
Catalogue number Size Status
TA1203242 Outer Diameter 12 mm In distribution
TBEA16140 Depth 16 mm In distribution
TA1602634 Outer Diameter 12 mm In distribution
TZBA0100F Outer Diameter 12 mm In distribution
TZBA0100H Outer Diameter 12 mm In distribution
TA1202329 Outer Diameter 12 mm In distribution
TZBA0100J Outer Diameter 12 mm In distribution
TZBA0100G Outer Diameter 12 mm In distribution
TA1203650 Outer Diameter 12 mm In distribution
TZBA02BC0 Outer Diameter 12 mm In distribution
TA1204160 Outer Diameter 12 mm In distribution
TBF016140 Depth 16 mm In distribution
TZBA0100E Outer Diameter 12 mm In distribution
TA1202025 Outer Diameter 12 mm In distribution
TA1205381 Outer Diameter 12 mm In distribution
TA1603441 Height 41 mm In distribution
TZBA0100B Outer Diameter 12 mm In distribution
TZBA0100D Outer Diameter 12 mm In distribution
TBEA18150 Depth 16 mm In distribution
TBEA14120 Depth 16 mm In distribution
TZBA0100A Outer Diameter 12 mm In distribution
TZBA0100C Outer Diameter 12 mm In distribution
TZBA0100K Outer Diameter 12 mm In distribution
TA1602027 Outer Diameter 12 mm In distribution
TBF014120 Depth 14 mm In distribution
TBB018150 Depth 16 mm In distribution
TA1201520 Outer Diameter 12 mm In distribution
TZBA02BB0 Outer Diameter 12 mm In distribution
TBB014120 Outer Diameter 12 mm In distribution
TZBA03000 In distribution
TA1206593 Outer Diameter 12 mm In distribution
TBF018150 Depth 18 mm In distribution
TZBA02BD0 Outer Diameter 12 mm In distribution
TA1203038 Outer Diameter 12 mm In distribution
TA1202834 Outer Diameter 12 mm In distribution
TBB016140 Depth 16 mm In distribution

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
K173324 2018-02-27
K160154 2016-05-13

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