2 catalogue numbers from 14-NL-004, listed by Jeil Medical Corporation, South Korea, under Plate, Cranioplasty, Preformed, Alterable. 2 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Jiangsu (1), Shanghai (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
Record
Regulatory record for Leforte Neuro System Bone Screw | Listed by | Jeil Medical Corporation, South Korea |
| FDA product code | GWO |
| Device type | Plate, Cranioplasty, Preformed, Alterable |
| Device class | Class 2 |
| Regulation | 21 CFR 882.5320 |
| Establishment | Manufacturer |
| 510(k) | K141452 |
| Record published | 2015-09-24 |
| Record revised | 2024-06-19 (version 6) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Sterilisation | Moist Heat or Steam Sterilization |
| Single use | Yes |
| 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.