VBR Omni™ Vertebral Body Replacement

VBR Omni, Ø 26 mm, height 72-131 mm, angle 16°

Registry build 21.09.26
3manufacturers in China registered for this device type
55catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (1), Jiangsu (1), Shandong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MQP
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for VBR Omni™ vertebral body replacement
Listed by Ulrich Gmbh & Co. KG, Germany
FDA product code MQP
Device type Spinal Vertebral Body Replacement Device
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Contract manufacturer, Manufacturer, Exporter
510(k) K012254
Record published 2016-08-30
Record revised 2025-06-06 (version 5)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for VBR Omni™ vertebral body replacement
Catalogue number Size Status
CS 2250-26-7216 In distribution
CS 2250-30-468 In distribution
CS 2250-30-328 In distribution
CS 2250-30-32 In distribution
CS 2250-26-464 In distribution
CS 2250-26-244 In distribution
CS 2250-22-244 In distribution
CS 2259-01 In distribution
CS 2250-19-328 In distribution
CS 2250-30-4612 In distribution
CS 2250-22-464 In distribution
CS 2250-26-24 In distribution
CS 2250-19-194 In distribution
CS 2250-19-19 In distribution
CS 2250-26-7220 In distribution
CS 2250-26-198 In distribution
CS 2250-30-3212 In distribution
CS 2250-19-10 In distribution
CS 2250-19-724 In distribution
CS 2250-22-324 In distribution
CS 2250-22-32 In distribution
CS 2250-22-194 In distribution
CS 2250-30-7212 In distribution
CS 2250-26-328 In distribution
CS 2250-22-19 In distribution
CS 2250-26-19 In distribution
CS 2250-22-468 In distribution
CS 2250-19-24 In distribution
CS 2250-19-468 In distribution
CS 2250-19-244 In distribution
CS 2250-26-194 In distribution
CS 2250-26-3212 In distribution
CS 2250-30-728 In distribution
CS 2250-30-7222 In distribution
CS 2250-19-15 In distribution
CS 2250-19-728 In distribution
CS 2250-26-4616 In distribution
CS 2250-26-32 In distribution
CS 2250-22-24 In distribution
CS 2250-22-3212 In distribution
CS 2250-30-324 In distribution
CS 2250-22-7216 In distribution
CS 2250-30-464 In distribution
CS 2250-26-468 In distribution
CS 2250-22-4612 In distribution
CS 2250-26-4612 In distribution
CS 2250-30-7216 In distribution
CS 2250-22-328 In distribution
CS 2250-26-248 In distribution
CS 2250-19-12 In distribution
CS 2250-30-4616 In distribution
CS 2250-19-46 In distribution
CS 2250-19-154 In distribution
CS 2250-19-32 In distribution
CS 2250-26-324 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CoRoent Nuvasive, Inc. 1,514
Capri™ Corpectomy Cage System VB Spine LLC 1,509
Aleutian® Interbody Systems VB Spine LLC 1,189
Fortify Globus Medical, Inc. 866
Matrixx System Nexxt Spine LLC 748
Ascend Alphatec Spine, Inc. 555
Zavation VBR Trial Zavation 548
Verte-Stack® Spinal System Medtronic Sofamor Danek, Inc. 484
Timberline® Lateral Interbody Fusion System Biomet Spine 470
Timberline Lateral Fusion System Biomet Spine 459
Novel Alphatec Spine, Inc. 447
Hawkeye™ Vertebral Body Replacement (VBR) Choice Spine, LP 368

Showing 12 of 683. All products under Spinal Vertebral Body Replacement Device

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K192117 2019-11-01
K090841 2009-10-05
K060416 2006-12-26

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