Template

Mobility TRIAL INSERT SZ 6 - 11mm

Registry build 21.09.26
21manufacturers in China registered for this device type
49catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (10), Shanghai (3), Zhejiang (2). 11 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HWT
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
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
Xinhua Healthcare Industry Co., Limited Zibo Shandong Contract manufacturer 30
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Sanbor Medical Xiamen, Inc. Xiamen Fujian Contract manufacturer 16
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5
Guangzhou Clean Medical Products Manufacturing Corp Guangzhou Guangdong Contract manufacturer 5
Shanghai Medical Instruments (Group) Ltd. Corp. Shanghai Shanghai Contract manufacturer 235

Showing 12 of 21. All 21 manufacturers in China registered for Template

Record

Regulatory record for Template
Listed by Depuy Intl., Ltd., United Kingdom
FDA product code HWT
Device type Template
Device class Class 1
Regulation 21 CFR 888.4800
Establishment Contract manufacturer, Contract steriliser, Specification developer, Manufacturer
Premarket notification Exempt
Record published 2018-09-24
Record revised 2020-12-21 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Template
Catalogue number Size Status
855505607 In distribution
855505203 In distribution
9611-56-000 In distribution
9608-10-001 In distribution
855505403 In distribution
9626-05-000 In distribution
855505505 In distribution
855505209 In distribution
9653-68-000 In distribution
855505205 In distribution
2299-01-089 In distribution
855505307 In distribution
9611-59-000 In distribution
9611-58-000 In distribution
855505107 In distribution
855505305 In distribution
2299-01-083 In distribution
855505507 In distribution
855505405 In distribution
2299-01-086 In distribution
9608-09-001 In distribution
855505309 In distribution
855505611 In distribution
855505409 In distribution
855505207 In distribution
9608-08-001 In distribution
855505109 In distribution
9626-00-000 In distribution
855505509 In distribution
1299-01-085 In distribution
855505503 In distribution
855505311 In distribution
9505-01-033 In distribution
855505605 In distribution
9626-01-000 In distribution
855505303 In distribution
855505407 In distribution
9626-03-000 In distribution
855539000 In distribution
9608-11-001 In distribution
855505511 In distribution
855505211 In distribution
855505609 In distribution
855505111 In distribution
855505105 In distribution
855505411 In distribution
9626-02-000 In distribution
855505603 In distribution
9611-57-000 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Attune Depuy (Ireland) 1,385
Template Exactech, Inc. 1,277
4WEB Medical 4WEB Inc. 991
Evolution® Microport Orthopedics Inc. 966
Template Zimmer, Inc. 792
Advance® Microport Orthopedics Inc. 644
Apex Knee System Omni Life Science, Inc. 635
Profemur® Microport Orthopedics Inc. 591
Link Instruments – Trial implants and size gauges Waldemar Link GmbH & Co. KG 549
Template Synthes Gmbh 516
Optetrak Logic Exactech, Inc. 512
Template Depuy Spine, Inc. 451

Showing 12 of 2,940. All products under Template

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K771710 1977-10-06
K771709 1977-10-06

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