Restoration

46 catalogue numbers from 1235-2-256, listed by Howmedica Osteonics Corp, United States, under Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer. 10 manufacturers in China are registered for this product code.

Registry build 21.09.26
10manufacturers in China registered for this device type
46catalogue numbers in this listing
4510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (2), Zhejiang (2). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWZ
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
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
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

Record

Regulatory record for Restoration
Listed by Howmedica Osteonics Corp, United States
FDA product code KWZ
Device type Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3310
Establishment Contract manufacturer, Contract steriliser, Specification developer, Manufacturer
Record published 2015-09-24
Record revised 2026-01-29 (version 8)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number
Sizes Outer diameter 50 to 56 mm; lumen/inner diameter 22.2 mm

Catalogue Numbers

Catalogue numbers for Restoration
Catalogue number Size Status
1235-2-256 Lumen/Inner Diameter 22.2 mm In distribution
6276-6-618 Stem Length: 317.0 Millimeter In distribution
6276-6-426 Distal Diameter: 26.0 Millimeter In distribution
6276-5-414 Distal Diameter: 14.0 Millimeter In distribution
6276-7-326 Distal Diameter: 26.0 Millimeter In distribution
6276-6-123 Distal Diameter: 23.0 Millimeter In distribution
6276-6-218 Distal Diameter: 18.0 Millimeter In distribution
6276-2-019 Diameter: 19.0 Millimeter In distribution
6276-6-619 Stem Length: 317.0 Millimeter In distribution
6276-7-215 Distal Diameter: 15.0 Millimeter In distribution
6276-8-621 Distal Diameter: 21.0 Millimeter In distribution
6276-6-521 Distal Diameter: 21.0 Millimeter In distribution
6276-1-219 Diameter: 19.0 Millimeter In distribution
6276-5-211 Distal Diameter: 11.0 Millimeter In distribution
6276-7-127 Distal Diameter: 27.0 Millimeter In distribution
6276-5-126 Distal Diameter: 26.0 Millimeter In distribution
6276-7-415 Distal Diameter: 15.0 Millimeter In distribution
6276-7-421 Stem Length: 115.0 Millimeter In distribution
6276-5-214 Distal Diameter: 14.0 Millimeter In distribution
6276-4-131 Diameter: 31.0 Millimeter In distribution
6276-5-025 Stem Length: 127.0 Millimeter In distribution
6276-8-219 Distal Diameter: 19.0 Millimeter In distribution
6276-1-031 Body Height: 0.0 Millimeter In distribution
1235-2-562 Outer Diameter 56.0 mm In distribution
6260-6-313 Stem Length: 165.0 Millimeter In distribution
6276-2-119 Diameter: 19.0 Millimeter In distribution
6276-5-411 Stem Length: 217.0 Millimeter In distribution
6276-5-419 Distal Diameter: 19.0 Millimeter In distribution
6276-3-008 Size: 8 In distribution
6276-1-019 Body Height: 0.0 Millimeter In distribution
6276-6-413 Distal Diameter: 13.0 Millimeter In distribution
6276-6-224 Stem Length: 167.0 Millimeter In distribution
6276-6-125 Stem Length: 167.0 Millimeter In distribution
6260-8-921 Distal Diameter: 21.0 Millimeter In distribution
6276-6-116 Distal Diameter: 16.0 Millimeter In distribution
6276-6-414 Stem Length: 217.0 Millimeter In distribution
6276-8-422 Distal Diameter: 22.0 Millimeter In distribution
6276-4-219 Diameter: 19.0 Millimeter In distribution
6276-5-017 Stem Length: 127.0 Millimeter In distribution
6276-6-014 Distal Diameter: 14.0 Millimeter In distribution
6276-4-327 Body Height: 30.0 Millimeter In distribution
6276-6-614 Distal Diameter: 14.0 Millimeter In distribution
6276-8-517 Stem Length: 267.0 Millimeter In distribution
6276-4-227 Diameter: 27.0 Millimeter In distribution
6276-6-617 Distal Diameter: 17.0 Millimeter In distribution
6276-5-022 Stem Length: 127.0 Millimeter In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DJO Surgical Encore Medical, L.P. 159
Instrument Howmedica Osteonics Corp 139
ZMR® Zimmer, Inc. 103
Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer Zimmer, Inc. 69
Arcos Modular Revision System Biomet Orthopedics 66
Pinnacle Depuy Orthopaedics, Inc. 52
System 12 Howmedica Osteonics Corp 47
Redapt Smith & Nephew, Inc. 43
R3 Smith & Nephew, Inc. 41
Trident Howmedica Osteonics Corp 38
Arcos Modular Revision Hip System Biomet Orthopedics 37
G7® Biomet Orthopedics 37

Showing 12 of 165. All products under Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K063445 2007-03-08
K063550 2007-03-08
K063552 2007-03-08
K061654 2006-07-07

Recalls

The FDA has not published a severity grade for these. 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
2026-07-30 Not classified Process change control Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to 12,156 US

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P960054 1997-06-19 S-ROM POLY-DIAL CONSTRAINED LINER Depuy, A Johnson & Johnson Co.

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