Leforte System Bone Screw

37 catalogue numbers from 20-MN-020, listed by Jeil Medical Corporation, South Korea, under Screw, Fixation, Bone. 31 manufacturers in China are registered for this product code.

Registry build 21.09.26
31manufacturers in China registered for this device type
37catalogue numbers in this listing
4510(k) clearances naming this product code

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 Leforte System Bone Screw
Listed by Jeil Medical Corporation, South Korea
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Manufacturer
510(k) K023365
Record published 2015-09-24
Record revised 2024-06-19 (version 7)

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 Leforte System Bone Screw
Catalogue number Size Status
20-MN-020 In distribution
12-MC-010 In distribution
27-MX-008 In distribution
15-MC-003 In distribution
12-MC-006 In distribution
24-MX-016 In distribution
12-MC-002 In distribution
19-MD-006 In distribution
27L-MX-014 In distribution
27L-MX-010 In distribution
27L-MX-016 In distribution
12-MC-008 In distribution
20-MN-018 In distribution
20-MN-004 In distribution
16-MD-005 In distribution
23-MN-008 In distribution
24-MX-010 In distribution
27L-MX-006 In distribution
24-MX-018 In distribution
27-MX-006 In distribution
24-MX-012 In distribution
24-MX-008 In distribution
12-MC-004 In distribution
12-MC-003 In distribution
24-MX-004 In distribution
24-MX-006 In distribution
20-MN-005 In distribution
27L-MX-012 In distribution
15-MC-006 In distribution
12-MC-005 In distribution
19-MD-004 In distribution
23-MN-006 In distribution
24-MX-020 In distribution
12-MC-012 In distribution
24-MX-014 In distribution
27-MX-012 In distribution
27L-MX-008 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
K233912 2024-03-11
K192417 2019-11-26
K091686 2009-11-13
K023365 2003-04-18

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