Matrix
TI Matrix Anatomic L-PL/3X3 H MEDIUM/REVERSIBLE/0.5MM Thick
3manufacturers in China registered for this device type
101catalogue numbers in this listing
4510(k) clearances naming this product code
1recall
Who Else Makes It
Concentrated in Jiangsu (1), Shanghai (1), Shaanxi (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 54 |
| LX Precision Shanghai Co Ltd | Shanghai | Shanghai | Contract manufacturer | 19 |
| Kontour (Xi’an) Medical Technology Co., Ltd. | Xi’An | Shaanxi | Contract manufacturer | 4 |
Record
| Listed by | Synthes Gmbh, Switzerland |
|---|---|
| FDA product code | JEY |
| Device type | Plate, Bone |
| Device class | Class 2 |
| Regulation | 21 CFR 872.4760 |
| Establishment | Specification developer, Manufacturer, Exporter |
| 510(k) | K083388 |
| Record published | 2015-09-14 |
| Record revised | 2025-02-06 (version 7) |
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 |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| 04.511.244.01 | In distribution | ||
| 04.511.218.05 | 5 | In distribution | |
| 04.511.208.05 | 5 | In distribution | |
| 04.511.246.01 | In distribution | ||
| 04.511.234.05 | 5 | In distribution | |
| 04.511.388 | In distribution | ||
| 04.511.328 | In distribution | ||
| 04.511.387 | In distribution | ||
| 04.511.206.01 | In distribution | ||
| 04.511.224.01 | In distribution | ||
| 04.511.323 | In distribution | ||
| 04.511.322 | In distribution | ||
| 04.511.329 | In distribution | ||
| 04.511.463 | In distribution | ||
| 04.511.214.05 | 5 | In distribution | |
| 04.511.242.01 | In distribution | ||
| 04.511.331 | In distribution | ||
| 04.511.235.01 | In distribution | ||
| 04.511.381 | In distribution | ||
| 04.511.325 | In distribution | ||
| 04.511.382 | In distribution | ||
| 04.511.238.01 | In distribution | ||
| 04.511.344 | In distribution | ||
| 04.511.308 | In distribution | ||
| 04.511.445 | In distribution | ||
| 04.511.342 | In distribution | ||
| 04.511.309 | In distribution | ||
| 04.511.386 | In distribution | ||
| 04.511.210.05 | 5 | In distribution | |
| 04.511.226.05 | 5 | In distribution | |
| 04.511.462 | In distribution | ||
| 04.511.341 | In distribution | ||
| 04.511.212.01 | In distribution | ||
| 04.511.218.01 | In distribution | ||
| 04.511.348 | In distribution | ||
| 04.511.347 | In distribution | ||
| 04.511.240.01 | In distribution | ||
| 04.511.389 | In distribution | ||
| 04.511.402 | In distribution | ||
| 04.511.349 | In distribution | ||
| 04.511.228.05 | 5 | In distribution | |
| 04.511.246.05 | 5 | In distribution | |
| 04.511.385 | In distribution | ||
| 04.511.214.01 | In distribution | ||
| 04.511.244.05 | 5 | In distribution | |
| 04.511.335 | In distribution | ||
| 04.511.242.05 | 5 | In distribution | |
| 04.511.224.05 | 5 | In distribution | |
| 04.511.326 | In distribution | ||
| 04.511.248.05 | 5 | In distribution | |
| 04.511.240.05 | 5 | In distribution | |
| 04.511.248.01 | In distribution | ||
| 04.511.404 | In distribution | ||
| 04.511.216.01 | In distribution | ||
| 04.511.444 | In distribution | ||
| 04.511.210.01 | In distribution | ||
| 04.511.225.01 | In distribution | ||
| 04.511.235.05 | 5 | In distribution | |
| 04.511.238.05 | 5 | In distribution | |
| 04.511.321 | In distribution | ||
| 04.511.225.05 | 5 | In distribution | |
| 04.511.303 | In distribution | ||
| 04.511.205.01 | In distribution | ||
| 04.511.324 | In distribution | ||
| 04.511.346 | In distribution | ||
| 04.511.204.01 | In distribution | ||
| 04.511.236.05 | 5 | In distribution | |
| 04.511.350 | In distribution | ||
| 04.511.301 | In distribution | ||
| 04.511.384 | In distribution | ||
| 04.511.421 | In distribution | ||
| 04.511.383 | In distribution | ||
| 04.511.212.05 | 5 | In distribution | |
| 04.511.464 | In distribution | ||
| 04.511.423 | In distribution | ||
| 04.511.334 | In distribution | ||
| 04.511.234.01 | In distribution | ||
| 04.511.305 | In distribution | ||
| 04.511.345 | In distribution | ||
| 04.511.228.01 | In distribution | ||
| 04.511.332 | In distribution | ||
| 04.511.206.05 | 5 | In distribution | |
| 04.511.422 | In distribution | ||
| 04.511.343 | In distribution | ||
| 04.511.307 | In distribution | ||
| 04.511.390 | In distribution | ||
| 04.511.306 | In distribution | ||
| 04.511.424 | In distribution | ||
| 04.511.216.05 | 5 | In distribution | |
| 04.511.327 | In distribution | ||
| 04.511.403 | In distribution | ||
| 04.511.302 | In distribution | ||
| 04.511.208.01 | In distribution | ||
| 04.511.226.01 | In distribution | ||
| 04.511.401 | In distribution | ||
| 04.511.205.05 | 5 | In distribution | |
| 04.511.461 | In distribution | ||
| 04.511.236.01 | In distribution | ||
| 04.511.304 | In distribution | ||
| 04.511.370 | In distribution | ||
| 04.511.204.05 | 5 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Plate, Bone | Stryker Leibinger Gmbh & Co. KG | 1,338 |
| Level ONE CMF | KLS-Martin L.P. | 1,160 |
| Medicon | Medicon eG. Chirurgiemechaniker-Genossenschaft | 843 |
| OsteoMed | Osteomed | 675 |
| Bioplate® | Bioplate, Inc. | 669 |
| Plate, Bone | Synthes Gmbh | 568 |
| Leforte System Bone Plate | Jeil Medical Corporation | 466 |
| CMF Visionare | Visionare LLC | 421 |
| Level ONE CMF, Sterile | KLS-Martin L.P. | 416 |
| Faico CMF System | Faico Medical, LLC | 361 |
| TraumaOne System | Biomet Microfixation | 357 |
| MatrixMANDIBLE | Synthes Gmbh | 277 |
Showing 12 of 152. All products under Plate, Bone
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K122647 | 2013-02-28 |
| K113567 | 2012-11-19 |
| K121574 | 2012-06-29 |
| K113251 | 2011-12-21 |
Recalls Naming This Product
2 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Synthes GMBH / Synthes Produktions GmbH | 510(k) number | 2020-06-16 | Class II | Under Investigation by firm | One lot of MatrixMIDFACE Emergency Screw 1.8mm, self-tapp, L 12mm, in Clip was packaged with a body clip etched with a 3 (representing 3mm) when it should have been packaged with body clip etched with a 12 (representing 12mm). | 41 units | 2022-04-15 |
| Synthes (USA) Products LLC | 510(k) number | 2015-06-24 | Class II | Process control | The affected part and lot numbers of the TI Matrix Pre-Bent Maxillary Plates may potentially have the incorrect laser etch denoting the orientation. | 31 | 2016-08-18 |
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2020-06-18 | Class II | Under Investigation by firm | One lot of MatrixNEURO 5mm screws was packaged in a body clip etched “4”, which indicated a 4mm screw. The outer package labeling correctly identifies a 5mm screw, but the body clop incorrectly identifies a shorter length for the screw. | 104 units | 2021-04-13 |
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.