XRL

XRL Medium Implant-Integrated 22MM-25MM HEIGHT/0 DEG-Sterile

Registry build 21.09.26
3manufacturers in China registered for this device type
150catalogue numbers in this listing
1510(k) clearance
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 XRL
Listed by Synthes Gmbh, Switzerland
FDA product code MQP
Device type Spinal Vertebral Body Replacement Device
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Manufacturer, Exporter
510(k) K103320
Record published 2015-09-14
Record revised 2026-05-11 (version 9)

Specifications

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

Catalogue Numbers

Catalogue numbers for XRL
Catalogue number Size Per pack Status
08.807.224S In distribution
08.807.214S In distribution
03.807.631 In distribution
08.807.324S In distribution
03.807.367 In distribution
03.807.368 In distribution
03.807.625 In distribution
08.807.243S In distribution
08.807.201S In distribution
03.807.522 In distribution
03.807.607 In distribution
08.807.341S In distribution
08.807.209S In distribution
08.807.245S In distribution
08.807.325S In distribution
03.807.641 In distribution
03.807.613 In distribution
03.807.609 In distribution
03.807.310 In distribution
03.807.503 In distribution
03.807.365 In distribution
08.807.222S In distribution
08.807.308S In distribution
03.807.524 In distribution
08.807.212S In distribution
03.807.382 In distribution
08.807.301S In distribution
03.807.542 In distribution
03.807.536 In distribution
03.807.348 In distribution
03.807.369 In distribution
03.807.608 In distribution
08.807.307S In distribution
08.807.321S In distribution
08.807.300.02S 2 In distribution
08.807.311S In distribution
08.807.203S In distribution
03.807.532 In distribution
03.807.545 In distribution
03.807.601 In distribution
08.807.204S In distribution
08.807.313S In distribution
03.807.535 In distribution
08.807.305S In distribution
08.807.332S In distribution
03.807.611 In distribution
03.807.332 In distribution
08.807.314S In distribution
08.807.213S In distribution
08.807.312S In distribution
08.807.304S In distribution
03.807.510 In distribution
03.807.509 In distribution
03.807.523 In distribution
08.807.244S In distribution
03.807.605 In distribution
03.807.507 In distribution
03.807.531 In distribution
03.807.356 In distribution
03.807.623 In distribution
03.807.633 In distribution
08.807.206S In distribution
03.807.544 In distribution
03.807.333 In distribution
03.807.642 In distribution
03.807.635 In distribution
08.807.234S In distribution
03.807.331 In distribution
03.807.604 In distribution
08.807.232S In distribution
08.807.310S In distribution
03.807.634 In distribution
03.807.606 In distribution
03.807.515 In distribution
08.807.200.02S 2 In distribution
08.807.343S In distribution
08.807.342S In distribution
08.807.334S In distribution
03.807.610 In distribution
03.807.645 In distribution
03.807.502 In distribution
03.807.543 In distribution
03.807.632 In distribution
03.807.612 In distribution
03.807.621 In distribution
08.807.306S In distribution
03.807.624 In distribution
03.807.311 In distribution
03.807.643 In distribution
08.807.208S In distribution
03.807.330 In distribution
08.807.211S In distribution
03.807.521 In distribution
08.807.210S In distribution
08.807.202S In distribution
08.807.221S In distribution
03.807.335 In distribution
03.807.508 In distribution
08.807.246S In distribution
03.807.315 In distribution
03.807.314 In distribution
08.807.207S In distribution
03.807.602 In distribution
03.807.384 In distribution
03.807.366 In distribution
08.807.345S In distribution
03.807.504 In distribution
03.807.533 In distribution
03.807.506 In distribution
03.807.511 In distribution
03.807.534 In distribution
08.807.315S In distribution
08.807.335S In distribution
03.807.513 In distribution
08.807.236S In distribution
03.807.364 In distribution
08.807.205S In distribution
08.807.303S In distribution
08.807.302S In distribution
08.807.241S In distribution
03.807.355 In distribution
08.807.215S In distribution
03.807.512 In distribution
08.807.331S In distribution
03.807.334 In distribution
03.807.541 In distribution
08.807.344S In distribution
03.807.501 In distribution
08.807.322S In distribution
08.807.333S In distribution
03.807.300 In distribution
08.807.235S In distribution
03.807.352 In distribution
08.807.223S In distribution
03.807.505 In distribution
03.807.313 In distribution
08.807.242S In distribution
03.807.351 In distribution
03.807.622 In distribution
08.807.231S In distribution
03.807.312 In distribution
03.807.644 In distribution
08.807.309S In distribution
03.807.546 In distribution
03.807.514 In distribution
03.807.603 In distribution
03.807.614 In distribution
08.807.233S In distribution
08.807.323S In distribution
03.807.615 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
K003836 2001-05-29

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of XRL
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Synthes Gmbh 510(k) number 2014-04-08 Class II Process control Two lots of the Synthes XRL Medium Trial-Central Body device were incorrectly etched with the incorrect dimensions for height. 3 2015-09-10

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