Artemis Proximal Femoral Nail System

ARTEMIS nail PF, Locking Screw, ø5 x 47.5

Registry build 21.09.26
31manufacturers in China registered for this device type
39catalogue numbers in this listing
2510(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 Artemis Proximal Femoral Nail System
Listed by GLW, Inc., United States
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K201379
Record published 2025-01-30
Record revised 2026-03-12 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, serial number

Catalogue Numbers

Catalogue numbers for Artemis Proximal Femoral Nail System
Catalogue number Size Status
T6-0300-075S In distribution
T6-0200-102S In distribution
T6-0300-045S In distribution
T6-0300-065S In distribution
T6-0200-085S In distribution
T6-0300-047S In distribution
T6-0300-040S In distribution
T6-0200-075S In distribution
T6-0300-035S In distribution
T6-0300-090S In distribution
T6-0300-030S In distribution
T6-0200-070S In distribution
T6-0200-115S In distribution
T6-0300-080S In distribution
T6-0300-095S In distribution
T6-0200-092S In distribution
T6-0300-105S In distribution
T6-0300-100S In distribution
T6-0200-110S In distribution
T6-0200-097S In distribution
T6-0300-032S In distribution
T6-0200-130S In distribution
T6-0300-025S In distribution
T6-0200-095S In distribution
T6-0300-085S In distribution
T6-0300-110S In distribution
T6-0300-070S In distribution
T6-0300-060S In distribution
T6-0200-120S In distribution
T6-0200-105S In distribution
T6-0300-042S In distribution
T6-0300-050S In distribution
T6-0200-080S In distribution
T6-0200-125S In distribution
T6-0200-090S In distribution
T6-0200-100S In distribution
T6-0300-027S In distribution
T6-0300-055S In distribution
T6-0300-037S 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
K223847 2023-01-25
K200291 2020-12-16

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