Redondo-L™

Redondo-L 45mm x 18mm x 8mm, 8 Deg. Redondo-L is intended to promote spinal fusion by acting as a spacer and holding bone graft. The implants have teeth on the superior and inferior…

Registry build 21.09.26

Redondo-L 45mm x 18mm x 8mm, 8 Deg. Redondo-L is intended to promote spinal fusion by acting as a spacer and holding bone graft. The implants have teeth on the superior and inferior surfaces and a central canal for receiving bone graft. These devices are available in a variety of lengths, widths, and heights to accommodate variations in pathology and patient anatomy. All Redondo-L implants are manufactured from PEEK OPTIMA®(polyetheretherketone, ASTM F-2026) with tantalum (ASTM F-560) radiographic wires and/or beads.

3manufacturers in China registered for this device type
10catalogue numbers in this listing

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 Redondo-L™
Listed by Seaspine Orthopedics Corporation, 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, Complaint-file establishment, Manufacturer
510(k) K103297
Record published 2015-09-24
Record revised 2025-10-24 (version 9)

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
Distribution end date 2016-09-02

Catalogue Numbers

Catalogue numbers for Redondo-L™
Catalogue number Size Status
36-5610 55mm x 18mm x 10mm, 0 degrees In distribution
36-5512 55mm x 18mm x 12mm, 8 degrees In distribution
36-4608 45mm x 18mm x 8mm, 0 degrees In distribution
36-5014 50mm x 18mm x 14mm, 8 degrees In distribution
36-5612 55mm x 18mm x 12mm, 0 degrees In distribution
36-5008 50mm x 18mm x 8mm, 8 degrees In distribution
36-5508 55mm x 18mm x 8mm, 8 degrees In distribution
93-6112 In distribution
36-5114 50mm x 18mm x 14mm, 0 degrees Withdrawn
36-4518 45mm x 18mm x 18mm, 8 degrees Withdrawn

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

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