EZ Frame

20 catalogue numbers from EF002450, listed by Wright Medical Technology, Inc., United States, under Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component. 17 manufacturers in China are registered for this product code.

Registry build 21.09.26
17manufacturers in China registered for this device type
20catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (4), Zhejiang (3). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KTT
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5

Showing 12 of 17. All 17 manufacturers in China registered for Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Record

Regulatory record for EZ Frame
Listed by Wright Medical Technology, Inc., United States
FDA product code KTT
Device type Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K130044
Record published 2015-10-24
Record revised 2026-06-24 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Sizes Height 5 to 10 mm
Distribution end date 2022-06-23

Catalogue Numbers

Catalogue numbers for EZ Frame
Catalogue number Size Status
EF002450 Size: 2mm In distribution
EF001650 6 Hole In distribution
EF410160 Size: 160mm In distribution
EF003775 Large In distribution
EF002500 In distribution
EF3005PK Height 5 mm In distribution
EF3010PK Height 10 mm In distribution
EF002000 In distribution
EF100000 Standard In distribution
EF003750 Standard In distribution
EF375000 Multipack of 5 In distribution
EF103750 Standard In distribution
EF10000L Large In distribution
EF004180 Size: 160mm In distribution
EF103775 Large In distribution
EF190002 In distribution
EF003005 Height 5 mm Withdrawn
EF003010 Height 10 mm Withdrawn
EF002550 Withdrawn
EF003700 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Smart Correction Wishbone Medical Inc. 1,534
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Synthes Gmbh 880
LCP Synthes Gmbh 355
Orthex External Fixation System Orthopediatrics, Corp 353
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Sterilmed, Inc. 325
CHS Smith & Nephew, Inc. 321
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Stryker Sustainability Solutions 277
Hoffmann Stryker GmbH 239
Orthex Orthopediatrics, Corp 231
Orthex Vilex IN Tennessee, Inc. 221
Omega Stryker GmbH 212
eZ-Fix Orthopediatrics, Corp 207

Showing 12 of 530. All products under Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K162033 2017-03-06

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