Construx – Mini Peek VBR

15mm W X 12mm L, 5° LORDOTIC - 11mm H IMPLANT, STERILE

Registry build 21.09.26
3manufacturers in China registered for this device type
32catalogue numbers in this listing
1recall

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 Construx – Mini Peek VBR
Listed by Orthofix US LLC, United States
FDA product code MQP
Device type Spinal Vertebral Body Replacement Device
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K202949
Record published 2026-07-17

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Construx – Mini Peek VBR
Catalogue number Size Status
47-4011SP In distribution
47-4005SP In distribution
47-3007SP In distribution
47-4012SP In distribution
47-4013SP In distribution
47-3112SP In distribution
47-4008SP In distribution
47-3010SP In distribution
47-3105SP In distribution
47-4111SP In distribution
47-4112SP In distribution
47-3113SP In distribution
47-4106SP In distribution
47-3011SP In distribution
47-4006SP In distribution
47-4105SP In distribution
47-3114SP In distribution
47-4014SP In distribution
47-3008SP In distribution
47-3107SP In distribution
47-3012SP In distribution
47-3106SP In distribution
47-4010SP In distribution
47-4110SP In distribution
47-3014SP In distribution
47-4113SP In distribution
47-4107SP In distribution
47-3005SP In distribution
47-4009SP In distribution
47-3110SP In distribution
47-4007SP In distribution
47-4114SP 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

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2009-11-19 Not classified Nonconforming Material/Component The Pillar SA Implant Insertion Instrument 49-1100 may experience resistance in turning the activation knob while releasing an implant after intra-operative positioning. 29 instruments 2010-02-02

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