Restoration

Anatomic Hemispherical Shell

Registry build 21.09.26
14manufacturers in China registered for this device type
109catalogue numbers in this listing
16510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Jiangsu (7), 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 LPH
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
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
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
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70

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

Record

Regulatory record for Restoration
Listed by Howmedica Osteonics Corp, United States
FDA product code LPH
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Device class Class 2
Regulation 21 CFR 888.3358
Establishment Contract manufacturer, Contract steriliser, Specification developer, Manufacturer
510(k) K102019
Record published 2015-09-24
Record revised 2026-01-29 (version 9)

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 46 to 80 mm; lumen/inner diameter 22.2 to 68 mm

Catalogue Numbers

Catalogue numbers for Restoration
Catalogue number Size Status
6276-6-121 Distal Diameter: 21.0 Millimeter In distribution
6276-5-013 Distal Diameter: 13.0 Millimeter In distribution
6276-6-417 Distal Diameter: 17.0 Millimeter In distribution
6260-8-212 Taper Connection: V40™ In distribution
6276-7-318 Stem Length: 235.0 Millimeter In distribution
6276-7-327 Distal Diameter: 27.0 Millimeter In distribution
504-02-78H-R Side: RIGHT In distribution
6276-4-127 Body Height: 10.0 Millimeter In distribution
5096-5015 Lumen/Inner Diameter 52.0 mm In distribution
6276-7-023 Distal Diameter: 23.0 Millimeter In distribution
5096-4625 Thickness: 25.0 Millimeter In distribution
5096-4615 Thickness: 15.0 Millimeter In distribution
6276-8-425 Stem Length: 217.0 Millimeter In distribution
6276-5-026 Stem Length: 127.0 Millimeter In distribution
6276-8-426 Stem Length: 217.0 Millimeter In distribution
5096-5815 Lumen/Inner Diameter 60.0 mm In distribution
6276-6-513 Distal Diameter: 13.0 Millimeter In distribution
5096-6225 Thickness: 25.0 Millimeter In distribution
504-02-60D-R Outer Diameter 60.0 mm In distribution
6276-6-412 Stem Length: 217.0 Millimeter In distribution
1235-2-561 Outer Diameter 56.0 mm In distribution
6276-5-415 Stem Length: 217.0 Millimeter In distribution
6276-8-521 Distal Diameter: 21.0 Millimeter In distribution
504-02-58D-L Outer Diameter 58.0 mm In distribution
6276-5-213 Distal Diameter: 13.0 Millimeter In distribution
504-02-54C-R Side: RIGHT In distribution
6260-6-820 Taper Connection: V40™ In distribution
5096-5425 Thickness: 25.0 Millimeter In distribution
6276-5-622 Stem Length: 317.0 Millimeter In distribution
5096-5415 Lumen/Inner Diameter 56.0 mm In distribution
5096-4620 Lumen/Inner Diameter 48.0 mm In distribution
6276-2-229 Diameter: 29.0 Millimeter In distribution
6276-6-020 Distal Diameter: 20.0 Millimeter In distribution
5096-6620 Outer Diameter 66.0 mm In distribution
6276-8-518 Stem Length: 267.0 Millimeter In distribution
6276-8-622 Distal Diameter: 22.0 Millimeter In distribution
6276-6-017 Stem Length: 127.0 Millimeter In distribution
5096-5420 Outer Diameter 54.0 mm In distribution
1235-2-602 Outer Diameter 60.0 mm In distribution
504-02-54C-L Outer Diameter 54.0 mm In distribution
504-02-70G-L Outer Diameter 70.0 mm In distribution
6276-5-422 Distal Diameter: 22.0 Millimeter In distribution
6276-6-212 Distal Diameter: 12.0 Millimeter In distribution
504-02-74H-R Outer Diameter 74.0 mm In distribution
6260-8-818 Stem Length: 203.0 Millimeter In distribution
6276-6-117 Stem Length: 167.0 Millimeter In distribution
6276-5-221 Distal Diameter: 21.0 Millimeter In distribution
504-02-64E-L Alpha Code: E In distribution
6276-6-517 Stem Length: 267.0 Millimeter In distribution
504-02-74H-L Alpha Code: H In distribution
6276-6-416 Distal Diameter: 16.0 Millimeter In distribution
6276-7-027 Stem Length: 155.0 Millimeter In distribution
5096-5825 Outer Diameter 58.0 mm In distribution
6276-5-120 Distal Diameter: 20.0 Millimeter In distribution
5096-6220 Outer Diameter 62.0 mm In distribution
6276-7-026 Stem Length: 155.0 Millimeter In distribution
504-02-62E-R Alpha Code: E In distribution
504-02-68F-R Outer Diameter 68.0 mm In distribution
6276-1-227 Body Height: 20.0 Millimeter In distribution
504-02-56D-L Outer Diameter 56.0 mm In distribution
6276-8-420 Stem Length: 217.0 Millimeter In distribution
6276-2-131 Diameter: 31.0 Millimeter In distribution
504-02-68F-L Outer Diameter 68.0 mm In distribution
1235-2-642 Outer Diameter 64.0 mm In distribution
504-02-64E-R Alpha Code: E In distribution
6260-8-820 Size: 8 In distribution
504-02-66F-R Outer Diameter 66.0 mm In distribution
6276-8-424 Stem Length: 217.0 Millimeter In distribution
504-02-72G-L Alpha Code: G In distribution
504-02-72G-R Side: RIGHT In distribution
504-02-70G-R Outer Diameter 70.0 mm In distribution
6276-5-215 Distal Diameter: 15.0 Millimeter In distribution
6276-6-019 Stem Length: 127.0 Millimeter In distribution
504-02-76H-L Side: LEFT In distribution
504-02-60D-L Alpha Code: D In distribution
6276-7-423 Distal Diameter: 23.0 Millimeter In distribution
6276-1-325 Body Height: 30.0 Millimeter In distribution
6276-5-520 Stem Length: 267.0 Millimeter In distribution
6276-6-422 Distal Diameter: 22.0 Millimeter In distribution
1235-2-482 Side: LEFT In distribution
6276-4-223 Diameter: 23.0 Millimeter In distribution
6276-6-214 Distal Diameter: 14.0 Millimeter In distribution
6260-8-517 Taper Connection: V40™ In distribution
504-02-66F-L Alpha Code: F In distribution
1235-2-262 Lumen/Inner Diameter 22.2 mm In distribution
6276-2-029 Diameter: 29.0 Millimeter In distribution
6276-5-617 Stem Length: 317.0 Millimeter In distribution
504-02-76H-R Side: RIGHT In distribution
6276-7-220 Distal Diameter: 20.0 Millimeter In distribution
6276-6-215 Stem Length: 167.0 Millimeter In distribution
504-02-78H-L Side: LEFT In distribution
5096-6625 Outer Diameter 66.0 mm In distribution
504-02-62E-L Alpha Code: E In distribution
6276-6-024 Stem Length: 127.0 Millimeter In distribution
1235-2-462 Outer Diameter 46.0 mm In distribution
6276-7-417 Distal Diameter: 17.0 Millimeter In distribution
6276-6-520 Distal Diameter: 20.0 Millimeter In distribution
504-02-58D-R Alpha Code: D In distribution
6276-1-221 Diameter: 21.0 Millimeter In distribution
6276-5-523 Distal Diameter: 23.0 Millimeter In distribution
5096-6615 Lumen/Inner Diameter 68.0 mm In distribution
504-02-80H-L Alpha Code: H In distribution
5096-5025 Thickness: 25.0 Millimeter In distribution
5096-6215 Thickness: 15.0 Millimeter In distribution
5096-5820 Lumen/Inner Diameter 60.0 mm In distribution
504-02-80H-R Outer Diameter 80.0 mm In distribution
5096-5020 Outer Diameter 50.0 mm In distribution
6276-8-222 Distal Diameter: 22.0 Millimeter In distribution
504-02-56D-R Alpha Code: D In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Initia Total Hip System Kyocera Medical Technologies, Inc. 1,000
DJO Surgical Encore Medical, L.P. 624
Pinnacle Depuy Orthopaedics, Inc. 613
Trilogy® Longevity® Zimmer, Inc. 564
Instrument Howmedica Osteonics Corp 369
InSitu Hip System Nextstep Arthropedix 368
Trilogy® Zimmer, Inc. 359
Kyocera Medical Technologies, Inc. Kyocera Medical Technologies, Inc. 298
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented Zimmer, Inc. 286
Bencox Hip System Corentec Co., Ltd. 286
OrthoMedFlex Orthomedflex LLC 257
Sterizo Total Hip System CPM Medical Consultants, LLC. 240

Showing 12 of 792. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K121308 2012-07-30
K101072 2011-04-11
K102019 2011-03-03
K090897 2009-10-23
K081171 2008-07-22
K062419 2006-11-15
K061434 2006-08-22
K061168 2006-07-18
K033716 2005-02-10
K032581 2003-10-09
K021911 2002-07-02
K020497 2002-03-04
K013475 2001-12-20
K010170 2001-04-18
K990849 1999-12-20
K993352 1999-11-19

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Restoration
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Howmedica Osteonics Corp 510(k) number 2014-08-15 Class II Under Investigation by firm The peel strength of the inner blister may have been below internal validated requirements. The strength of the seal is directly related to long term shelf life of the sterile barrier. 1,147 in total 2018-01-05

Recalls

34 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
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 3 units
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 45 units
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 0
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 48 units
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 0
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 225 units
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 0
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 0
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 0
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 0
2024-02-27 Class II Under Investigation by firm The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell 0
2021-12-21 Class II Under Investigation by firm There is a potential for the outer Tyvek lid to de-bond from the sealed package. 8 units
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 4895 2021-11-15
2020-04-16 Class II Packaging The Stryker Restoration Anatomic Shell (RAS) may fall off its post within its inner packaging which can result in the device loose in the package with coating debris. 2021-11-15
2019-10-03 Class II Employee error Boxes of the 6-Petal X-Change Wall Mesh Small (Part # 0942-8-025) contain the 4-Petal X-Change Wall Mesh Small (Part # 0942-8-015) 40 units 2022-04-21
2017-07-21 Class II Process control Inner and outer sterile barriers not fully sealed. 255 2020-03-12
2017-07-21 Class II Process control Inner and outer sterile barriers not fully sealed. 255 2020-03-12
2016-06-03 Class II Process design Impactors do not meet the required sterility assurance level (SAL) of 10-6 when using the recommended steam sterilization method. 1,864 units 2018-08-01
2015-09-08 Class II Process design Complaints that the femoral head could not be assembled with its corresponding V40 stem trunnion at the time of surgery. 201 2017-07-25
2015-06-25 Class II Nonconforming Material/Component it was discovered that item 623-10-36I Lot 3Y0KHP, although meeting all device specifications, was determined to be unacceptable due to a documentation issue. However the parts were inadvertently shipped to the field. 16 units 2017-08-30
2007-09-28 Not classified Packaging process control Mis-labeling: The warning label “Do not use with heads more than +10mm offset” does not appear on 127 degree stem boxes. 30 2008-10-27
2007-09-28 Not classified Packaging process control Mis-labeling: The warning label “Do not use with heads more than +10mm offset” does not appear on 127 degree stem boxes. 46 2008-10-27
2007-09-28 Not classified Other Mis-labeling: An error on page 4 of the Hipstar protocol was found. In the table for compatible Heads, the 40 mm diameter heads with a Neck Length of +12 should have been omitted. 192 protocols 2008-09-05
2007-09-28 Not classified Packaging process control Mis-labeling: The warning label “Do not use with heads more than +10mm offset” does not appear on 127 degree stem boxes. 44 2008-10-27
2007-09-28 Not classified Packaging process control Mis-labeled: The warning label “Do not use with heads more than +10mm offset” does not appear on 127 degree stem boxes. 59 2008-10-27

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
P880025 1991-12-04 AML(R) POROCOAT(R) ACETABULAR CUP PROSTHESIS Depuy Intl., Ltd.
P880076 1991-06-17 WHITESIDE EPS(TM) FEMORAL HIP PROSTHESIS Dow Corning Wright
P850061 1991-03-08 BIAS(R) FIBER METAL TOTAL HIP SYSTEM Zimmer, Inc.

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