Link Instrument

Adapterbase for prosthesis head

Registry build 21.09.26
14manufacturers in China registered for this device type
38catalogue numbers in this listing
2510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (8), Shanghai (2), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MEH
Manufacturer City Province Registered as Device types
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
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Xian Airfoil Technology Co., Ltd. Xian Shaanxi Contract manufacturer 8
Lincotek (Wuxi) Co., Ltd. Wuxi Jiangsu Contract manufacturer 7
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing Contract manufacturer 7
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54

Showing 12 of 14. All 14 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

Record

Regulatory record for Link Instrument
Listed by Waldemar Link GmbH & Co. KG, Germany
FDA product code MEH
Device type Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Device class Class 2
Regulation 21 CFR 888.3353
Establishment Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K161840
Record published 2018-11-23
Record revised 2024-09-11 (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, manufacturing date

Catalogue Numbers

Catalogue numbers for Link Instrument
Catalogue number Size Status
175-200/11 In distribution
165-111/12 In distribution
165-111/20 In distribution
175-200/10 In distribution
175-201/21 In distribution
184-350/56 In distribution
175-200/09 In distribution
184-350/44 In distribution
184-330/00 In distribution
175-201/14 In distribution
165-111/14 In distribution
165-111/11 In distribution
175-201/02 In distribution
175-200/08 In distribution
175-201/07 In distribution
175-200/16 In distribution
175-201/17 In distribution
184-350/42 In distribution
165-111/13 In distribution
175-200/05 In distribution
175-200/21 In distribution
184-350/52 In distribution
184-362/00 In distribution
175-201/12 In distribution
175-200/04 In distribution
175-200/18 In distribution
175-200/20 In distribution
175-201/11 In distribution
175-200/22 In distribution
165-111/15 In distribution
175-201/19 In distribution
175-200/07 In distribution
184-350/54 In distribution
165-111/09 In distribution
175-200/15 In distribution
184-360/00 In distribution
184-350/58 In distribution
175-201/06 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Alteon Exactech, Inc. 326
Novation Exactech, Inc. 317
Pinnacle Depuy Orthopaedics, Inc. 305
SP-CL Hip Stem Waldemar Link GmbH & Co. KG 219
Emperion Smith & Nephew, Inc. 201
MobileLink Acetabular Cup System Waldemar Link GmbH & Co. KG 154
Instrument Howmedica Osteonics Corp 145
Restoration Howmedica Osteonics Corp 144
Mfinity Femoral System Medacta International SA 138
Echelon Smith & Nephew, Inc. 134
Trinity Acetabular Hip System Corin Limited 128
Redapt Smith & Nephew, Inc. 127

Showing 12 of 805. All products under Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K250375 2025-11-05
K171273 2018-01-19

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Link Instrument
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Waldemar Link GmbH & Co. KG 510(k) number 2018-12-04 Class II Employee error The internal labeling included with these implants may include incorrect part numbers and could result in these incorrect labels being added to patient records. 30 2020-06-05
Waldemar Link GmbH & Co. KG 510(k) number 2018-12-04 Class II Employee error The internal labeling included with these implants may include incorrect part numbers and could result in these incorrect labels being added to patient records. 31 2020-06-05

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