MobiliT Cup

MobiliT Cementless spray titanium + HA acetabular cup with flanges – Dia. 68

Registry build 21.09.26
14manufacturers in China registered for this device type
73catalogue numbers in this listing
1510(k) clearance
14recalls 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 MobiliT Cup
Listed by Corin Limited, United Kingdom
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 Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K191831
Record published 2022-12-08
Record revised 2026-02-09 (version 3)

Specifications

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

Catalogue Numbers

Catalogue numbers for MobiliT Cup
Catalogue number Size Status
HDM768 In distribution
MDM066 In distribution
MDM048A In distribution
HDM554 In distribution
MDM156 In distribution
MDM166 In distribution
MDM052A In distribution
MDM044 In distribution
MDM352 In distribution
HDM650 In distribution
MDM016 In distribution
MDM142 In distribution
HDM2850 In distribution
MDM264 In distribution
HDM760 In distribution
MDM052 In distribution
MDM158 In distribution
HDM762 In distribution
HDM560 In distribution
HDM652 In distribution
HDM852 In distribution
MDM020 In distribution
MDM250 In distribution
MDM050 In distribution
MDM006Z2 In distribution
HDM858 In distribution
MDM266 In distribution
MDM068 In distribution
HDM2852 In distribution
MDM244 In distribution
MDM246 In distribution
HDM660 In distribution
MDM268 In distribution
MDM360 In distribution
HDM2854 In distribution
MDM252 In distribution
HDM646 In distribution
MDM144 In distribution
MDM015 In distribution
MDM062A In distribution
HDM664 In distribution
HDM854 In distribution
HDM850 In distribution
HDM856 In distribution
HDM868 In distribution
MDM362 In distribution
MDM004Z2 In distribution
HDM2856 In distribution
MDM044A In distribution
HDM752 In distribution
MDM262 In distribution
HDM548 In distribution
VDV755 In distribution
HDM546 In distribution
MDM019 In distribution
MCT800 In distribution
HDM668 In distribution
MDM068A In distribution
HDM750 In distribution
HDM544 In distribution
MDM011 In distribution
VDV735 In distribution
MDM001 In distribution
MDM060A In distribution
MDM008 In distribution
MDM254 In distribution
HDM764 In distribution
HDM2868 In distribution
MDM050A In distribution
MDM056 In distribution
HDM666 In distribution
HDM2242 In distribution
MDM356 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
K261576 2026-08-10

Recalls

14 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2021-07-28 Class II Storage The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices. 5 units 2024-06-12
2021-07-28 Class II Storage The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices. 2 2024-06-12
2021-07-28 Class II Storage The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices. 2 units 2024-06-12
2021-07-28 Class II Storage The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices. 4 2024-06-12
2021-07-28 Class II Storage The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices. 5 2024-06-12
2021-07-28 Class II Storage The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices. 2 units 2024-06-12
2021-07-28 Class II Storage The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices. 1 unit 2024-06-12
2021-07-28 Class II Storage The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices. 6 units 2024-06-12
2021-07-28 Class II Storage The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices. 1 unit 2024-06-12
2021-07-28 Class II Storage The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices. 2 units 2024-06-12
2021-05-06 Class II Under Investigation by firm Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice versa. 1 unit 2023-07-05
2021-05-06 Class II Under Investigation by firm Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice versa. 4 units 2023-07-05
2021-01-25 Class II Labeling mix-ups The size indicated on the labeling on the outer packaging, on the inner packaging, and on the patient stickers inside the packaging is incorrect: the Trinity Biolox Delta Ceramix Head 32XL is labeled as 36XL and vice-versa. 23 units 2022-11-23
2021-01-25 Class II Labeling mix-ups The size indicated on the labeling on the outer packaging, on the inner packaging, and on the patient stickers inside the packaging is incorrect: the Trinity Biolox Delta Ceramix Head 32XL is labeled as 36XL and vice-versa. 23 units 2022-11-23

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