Ezstart

Ezstart Interference Screw, 10MM X 20MM, Titanium

Registry build 21.09.26
31manufacturers in China registered for this device type
35catalogue 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 Ezstart
Listed by ConMed Corporation, United States
FDA product code HWC
Device type Screw, Fixation, Bone
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K182955
Record published 2025-05-13
Record revised 2026-04-01 (version 9)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Radiation Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Packaging Carton
Sizes Width 6 to 10 mm; length 15 to 30 mm
Distribution end date 2026-04-01

Catalogue Numbers

Catalogue numbers for Ezstart
Catalogue number Size Status
EZ0620T Width 6 mm In distribution
EZ1020T Width 10 mm In distribution
EZ1015T Width 10 mm In distribution
EZ0815T Length 15 mm In distribution
EZ0915T Length 15 mm In distribution
EZ1030T Width 10 mm In distribution
EZ0925T Length 25 mm In distribution
EZ0830T Length 30 mm In distribution
EZ0730T Length 30 mm In distribution
EZ0715T Width 7 mm In distribution
EZ0720T Width 7 mm In distribution
EZ0920T Width 9 mm In distribution
EZ0930T Width 9 mm In distribution
EZ0615T Width 6 mm In distribution
EZ0825T Length 25 mm In distribution
EZ0820T Length 20 mm In distribution
EZ0725T 7mm x 25mm In distribution
EZ1025T Width 10 mm In distribution
EZ1025T 10mm x 25mm Withdrawn
EZ0720T 7mm x 20mm Withdrawn
EZ0615T 6mm x 15mm\ Withdrawn
EZ0715T 7mm x 15mm Withdrawn
EZ0925T 9mm x 25mm Withdrawn
EZ0820T 8mm x 20mm Withdrawn
EZ0830T 8mm x 30mm Withdrawn
EZ1015T 10mm x 15mm Withdrawn
EZ0920T 9mm x 20mm Withdrawn
EZ0815T 8mm x 15mm Withdrawn
EZ0930T 9mm x 30mm Withdrawn
EZ1030T 10mm x 30mm Withdrawn
EZ0730T 7mm x 30mm Withdrawn
EZ0620T 6mm x 20mm Withdrawn
EZ0825T 8mm x 25mm Withdrawn
EZ1020T 10mm x 20mm Withdrawn
EZ0915T 9mm x 15mm Withdrawn

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
K182955 2019-01-22

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