MatrixMIDFACE

TI Matrixmidface Oblique L-PL 15MM/2X2 H/RIGHT/0.7MM Thick

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue numbers in this listing

Who Else Makes It

Concentrated in Jiangsu (1), Shanghai (1), Fujian (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DZL
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
Dentalmaster (Xiamen) Medical Technology Co., Ltd. Xiamen Fujian Manufacturer 1

Record

Regulatory record for MatrixMIDFACE
Listed by Synthes (U.S.A.) LP
FDA product code DZL
Device type Screw, Fixation, Intraosseous
Device class Class 2
Regulation 21 CFR 872.4880
510(k) K050608
Record published 2015-09-14
Record revised 2025-06-09 (version 8)

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
Distribution end date 2020-06-28

Catalogue Numbers

Catalogue numbers for MatrixMIDFACE
Catalogue number Size Status
SD445.003 Withdrawn
SD445.002 Withdrawn
SD445.004 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
OsteoMed Osteomed 1,295
Faico CMF System Faico Medical, LLC 540
Neoface Neoortho Produtos Ortopédicos S/A 181
CMF Visionare Visionare LLC 155
Universal Mandible AXS Stryker Leibinger Gmbh & Co. KG 148
Tandry CMF Plate System Microware Precision Co., Ltd. 140
Screw, Fixation, Intraosseous Synthes Gmbh 132
Level ONE CMF KLS-Martin L.P. 71
MatrixMIDFACE Synthes Gmbh 65
PlusDrive Synthes Gmbh 52
Universal 2.0 MP AXS Stryker Leibinger Gmbh & Co. KG 51
MCI – Medical Concept Innovation, Inc. MCI Medical Concept Innovation Inc. 49

Showing 12 of 92. All products under Screw, Fixation, Intraosseous

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 MatrixMIDFACE
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

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