Syntec Osteo-Plate and Screw Fixation

Cancellous Screw/Fully Threadφ4.0 x L16mm

Registry build 21.09.26
31manufacturers in China registered for this device type
51catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (15), Shanghai (5), Zhejiang (3). 19 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HWC
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11

Showing 12 of 31. All 31 manufacturers in China registered for Screw, Fixation, Bone

Record

Regulatory record for Syntec Osteo-plate and screw Fixation
Listed by Syntec Scientific Corp., Taiwan
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Contract manufacturer, Manufacturer
510(k) K092889
Record published 2023-06-16
Record revised 2024-02-19 (version 2)

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

Catalogue Numbers

Catalogue numbers for Syntec Osteo-plate and screw Fixation
Catalogue number Size Status
202818 In distribution
204875 In distribution
204816 In distribution
202834 In distribution
202816 In distribution
204885 In distribution
202830 In distribution
204832 In distribution
202808 In distribution
204828 In distribution
206016 In distribution
204838 In distribution
204822 In distribution
202806 In distribution
204826 In distribution
202812 In distribution
204834 In distribution
204840 In distribution
204830 In distribution
204845 In distribution
202822 In distribution
202824 In distribution
204865 In distribution
204820 In distribution
204890 In distribution
202838 In distribution
202820 In distribution
204905 In distribution
204850 In distribution
202832 In distribution
204855 In distribution
204818 In distribution
204836 In distribution
202810 In distribution
204814 In distribution
204812 In distribution
202826 In distribution
204870 In distribution
204900 In distribution
202840 In distribution
202828 In distribution
202836 In distribution
204910 In distribution
204895 In distribution
204860 In distribution
206018 In distribution
204824 In distribution
204880 In distribution
204810 In distribution
202814 In distribution
206014 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Screw, Fixation, Bone Synthes Gmbh 3,975
Aptus Medartis Inc. 3,623
Acumed Acumed LLC 3,187
Arthrex® Arthrex, Inc. 2,781
OsteoMed Osteomed 2,764
Screw, Fixation, Bone AAP Implantate AG 2,176
Screw, Fixation, Bone Zimmer, Inc. 1,993
Arix System Bone Screw Jeil Medical Corporation 1,875
Cannulated Screw System + Tyber Medical 1,814
Cannulated Compression Headless Screw Tyber Medical 1,621
Microware Bone Plates and Bone Screws Microware Precision Co., Ltd. 1,601
Anthem Globus Medical, Inc. 1,538

Showing 12 of 5,775. All products under Screw, Fixation, Bone

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K983495 1998-12-16

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