Restoration ADM/MDM X3 Insert

2 catalogue numbers from 7236-2-848, listed by Howmedica Osteonics Corp, United States, under Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented. 15 manufacturers in China are registered for this product code.

Registry build 21.09.26
15manufacturers in China registered for this device type
2catalogue numbers in this listing
24510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (8), Shanghai (3), Zhejiang (2). 10 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LZO
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
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
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

Showing 12 of 15. All 15 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Record

Regulatory record for Restoration ADM/MDM X3 Insert
Listed by Howmedica Osteonics Corp, United States
FDA product code LZO
Device type Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
Device class Class 2
Regulation 21 CFR 888.3353
Establishment Contract manufacturer, Contract steriliser, Specification developer, Manufacturer
Record published 2019-11-12
Record revised 2026-01-29 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Lumen/inner diameter 28 mm; outer diameter 42 to 46 mm

Catalogue Numbers

Catalogue numbers for Restoration ADM/MDM X3 Insert
Catalogue number Size Status
7236-2-848 Lumen/Inner Diameter 28.0 mm In distribution
7236-2-852 Alpha Code: F In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Libertas Maxx Orthopedics Inc. 1,832
Redapt Smith & Nephew, Inc. 326
Bencox Hip System Corentec Co., Ltd. 295
M-Vizion Femoral Revision System Medacta International SA 289
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Zimmer, Inc. 280
Profemur® Microport Orthopedics Inc. 229
DJO Surgical Encore Medical, L.P. 162
Instrument Howmedica Osteonics Corp 152
Alteon Exactech, Inc. 151
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Exactech, Inc. 136
Resolve Modular Revision Hip Stem United Orthopedic Corp. 136
Wagner SL Revision® Zimmer, Inc. 133

Showing 12 of 691. All products under Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K103233 2011-02-03
K071082 2007-09-13
K070885 2007-05-16
K063616 2006-12-20
K052718 2005-10-27
K051737 2005-07-19
K051738 2005-07-19
K051588 2005-07-12
K041940 2005-02-11
K041170 2004-11-09
K040734 2004-08-25
K031217 2003-05-23
K023901 2003-01-28
K022403 2002-10-17
K022549 2002-09-23
K022555 2002-08-26
K013106 2002-04-03
K003379 2000-11-30
K003391 2000-11-28
K003413 2000-11-24
K002320 2000-09-14
K001449 2000-08-04
K993889 2000-02-11
K991952 1999-06-29

Recalls

3 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
2022-01-14 Class II Under Investigation by firm Potential product mix where the size and/or offset of the Biolox delta Ceramic V40 Femoral Head inside the package does not match the package labeling 39 units Updated: 40 units
2022-01-14 Class II Under Investigation by firm Potential product mix where the size and/or offset of the Biolox delta Ceramic V40 Femoral Head inside the package does not match the package labeling 92 units Update: 40 units
2012-04-02 Class II Device Design Stryker Orthopaedics has become aware of a burr, or a metal shaving, observed in the internal threaded portion of the Cone Body Trial. The typical size of the shaving observed was 1-2 mm in length and 0.037 mm squared in cross section. 10, 983 units 2013-06-13
2011-06-03 Not classified Labeling False and Misleading Stryker Orthopaedics has become ware that there is the potential for interpretation of the product labeling which may lead to an incorrect implant being used. 13,263 units 2013-11-13
2011-06-03 Not classified Labeling False and Misleading Stryker Orthopaedics has become ware that there is the potential for interpretation of the product labeling which may lead to an incorrect implant being used. 1677 units 2013-11-13
2011-06-03 Not classified Labeling False and Misleading Stryker Orthopaedics has become ware that there is the potential for interpretation of the product labeling which may lead to an incorrect implant being used. 1951 units 2013-11-13
2009-12-30 Not classified Process control The Restoration Modular Hip Stem may have two different package labels. The 14 mm diameter stem may be labeled with both a size 14 mm diameter and a 26 mm diameter. 1 2012-09-14
2009-08-31 Not classified Error in labeling Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone. 2,876 2013-07-17
2009-08-31 Not classified Error in labeling Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone. 5,670 2013-07-17
2009-08-31 Not classified Error in labeling Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone. 3,510 2013-07-17
2009-08-31 Not classified Error in labeling Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone. 978 2013-07-17
2009-08-31 Not classified Error in labeling Certain surgical protocols do not provide specific instructions for initiating power to the calcar planer prior to engagement with bone. 1,362 2013-07-17
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203- all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties. 2010-07-27
2009-06-26 Not classified Nonconforming Material/Component The raw material used in the production of the Unipolar adaptor sleeve and the Restoration modular products are not affected by the previously mentioned metallurgical non-compliance issue. however, poor process controls demonstrated by thi 203 – all varieties 2010-07-27

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