Biolox

Anatomic Universal Taper Femoral Head

Registry build 21.09.26
15manufacturers in China registered for this device type
34catalogue 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 Biolox
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
510(k) K234025
Record published 2015-09-24
Record revised 2025-09-18 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Outer diameter 22.2 to 44 mm

Catalogue Numbers

Catalogue numbers for Biolox
Catalogue number Size Status
18-3600 Taper Connection: C-TPR In distribution
6570-0-222 Neck Length: 3.0 Millimeter In distribution
18-3675 Taper Connection: C-TPR In distribution
18-32-3 Neck Length: -2.5 Millimeter In distribution
6570-0-028 Neck Length: -4.0 Millimeter In distribution
18-36-3 Taper Connection: C-TPR In distribution
6570-0-228 Outer Diameter 28.0 mm In distribution
6570-0-032 Outer Diameter 32.0 mm In distribution
6570-0-328 Outer Diameter 28.0 mm In distribution
6570-0-232 Outer Diameter 32.0 mm In distribution
18-2800 Taper Connection: C-TPR In distribution
6570-0-132 Outer Diameter 32.0 mm In distribution
6570-0-236 Neck Length: 5.0 Millimeter In distribution
6570-0-736 Outer Diameter 36.0 mm In distribution
18-3225 Neck Length: 2.5 Millimeter In distribution
18-28-3 Taper Connection: C-TPR In distribution
18-3625 Taper Connection: C-TPR In distribution
6519-1-044 Outer Diameter 44.0 mm In distribution
18-2805 Taper Connection: C-TPR In distribution
6570-0-036 Outer Diameter 36.0 mm In distribution
6570-0-022 Neck Length: 0.0 Millimeter In distribution
18-3200 Taper Connection: C-TPR In distribution
6519-1-036 Outer Diameter 36.0 mm In distribution
6570-0-128 Neck Length: 0.0 Millimeter In distribution
6519-1-032 Outer Diameter 32.0 mm In distribution
6519-1-028 Outer Diameter 28.0 mm In distribution
18-36-5 Taper Connection: C-TPR In distribution
18-2825 Neck Length: 2.5 Millimeter In distribution
18-3605 Outer Diameter 36.0 mm In distribution
6519-1-040 Outer Diameter 40.0 mm In distribution
18-3205 Outer Diameter 32.0 mm In distribution
6570-0-536 Outer Diameter 36.0 mm In distribution
6570-0-436 Neck Length: -2.5 Millimeter In distribution
6570-0-136 Neck Length: 0.0 Millimeter 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 Naming This Product

2 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Biolox
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Howmedica Osteonics Corp UDI-DI 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
Howmedica Osteonics Corp UDI-DI 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

Recalls

1 of these is 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
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