Catalogue number 44-040, listed by Icotec AG, Switzerland, under Spinal Vertebral Body Replacement Device. 3 manufacturers in China are registered for 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.
Record
Regulatory record for Kong-TL VBR System, Inserter for VBR | Listed by | Icotec AG, Switzerland |
| FDA product code | MQP |
| Device type | Spinal Vertebral Body Replacement Device |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3060 |
| Establishment | Complaint-file establishment, Manufacturer |
| Record published | 2020-06-19 |
| Record revised | 2025-08-07 (version 4) |
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, manufacturing date |
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.