Reflection

Reflection Xlpe 28MM Inner Diameter 0 Degree Lateralized +4MM 58-60MM Outer Diameter Size G ETO

Registry build 21.09.26
14manufacturers in China registered for this device type
168catalogue numbers in this listing
32510(k) clearances naming this product code
4recalls 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 Reflection
Listed by Smith & Nephew, Inc., 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, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K022556
Record published 2015-08-30
Record revised 2025-10-08 (version 8)

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, expiry date
Storage Special storage condition: : –
Distribution end date 2022-03-17

Catalogue Numbers

Catalogue numbers for Reflection
Catalogue number Size Status
71332571 In distribution
71333399 In distribution
71332561 In distribution
71333356 In distribution
71353255 In distribution
71934725 In distribution
71334576 In distribution
71334573 In distribution
71332526 In distribution
71333355 In distribution
71923740 In distribution
71331082 In distribution
71923738 In distribution
71334551 In distribution
71333397 In distribution
71352246 In distribution
71333346 In distribution
71352849 In distribution
71333499 In distribution
71332541 In distribution
71335158 In distribution
71333347 In distribution
743070 In distribution
71331315 In distribution
71331089 In distribution
71330046 In distribution
71353252 In distribution
71331068 In distribution
71331066 In distribution
71335166 In distribution
71331064 In distribution
71331088 In distribution
71334515 In distribution
71331314 In distribution
71339946 In distribution
71333349 In distribution
71352249 In distribution
71333496 In distribution
71331311 In distribution
71352858 In distribution
71333345 In distribution
71332528 In distribution
71742062 In distribution
71335152 In distribution
746615 In distribution
71333398 In distribution
71335160 In distribution
71331072 In distribution
71331090 In distribution
71333446 In distribution
71334502 In distribution
71332551 In distribution
71331316 In distribution
71352861 In distribution
71333449 In distribution
71332531 In distribution
71333408 In distribution
71334575 In distribution
71331056 In distribution
71334523 In distribution
71334524 In distribution
71921436 In distribution
71333447 In distribution
71335162 In distribution
71352243 In distribution
71930640 In distribution
71352258 In distribution
71352846 In distribution
71352255 In distribution
71333498 In distribution
71930638 In distribution
71330466 In distribution
71352252 In distribution
71921435 In distribution
71930643 In distribution
71331062 In distribution
71332536 In distribution
71333396 In distribution
71930655 In distribution
71353258 In distribution
71353261 In distribution
71331091 In distribution
71334512 In distribution
71334526 In distribution
71334527 In distribution
71331060 In distribution
71332556 In distribution
71332538 In distribution
71335156 In distribution
71335154 In distribution
71352261 In distribution
71934727 In distribution
71331070 In distribution
71921434 In distribution
71930645 In distribution
71333348 In distribution
71335150 In distribution
71930649 In distribution
71352852 In distribution
71331058 In distribution
71923739 In distribution
71333445 In distribution
71335164 In distribution
71352240 In distribution
71930642 In distribution
71335168 In distribution
71352855 In distribution
71334574 In distribution
71930639 In distribution
71333448 In distribution
71334514 In distribution
71332566 In distribution
71353249 In distribution
71930644 In distribution
71333395 In distribution
71333497 In distribution
71333368 In distribution
71334562 In distribution
71332546 In distribution
71923734 In distribution
71334525 In distribution
71334513 In distribution
71930641 In distribution
71333357 In distribution
71333495 In distribution
71934726 In distribution
743052 Withdrawn
71335456 Withdrawn
71921442 Withdrawn
71335262 Withdrawn
71335256 Withdrawn
743060 Withdrawn
71335464 Withdrawn
71335480 Withdrawn
71335258 Withdrawn
71335476 Withdrawn
740068 Withdrawn
71925456 Withdrawn
71335472 Withdrawn
740070 Withdrawn
743068 Withdrawn
71335462 Withdrawn
71335254 Withdrawn
740048 Withdrawn
743044 Withdrawn
71923737 Withdrawn
71335454 Withdrawn
71923735 Withdrawn
71921443 Withdrawn
743064 Withdrawn
71335260 Withdrawn
71921441 Withdrawn
71335266 Withdrawn
71335252 Withdrawn
743066 Withdrawn
71335268 Withdrawn
71335470 Withdrawn
743062 Withdrawn
71335474 Withdrawn
743058 Withdrawn
71335250 Withdrawn
71923736 Withdrawn
71335468 Withdrawn
71335460 Withdrawn
71335478 Withdrawn
71335458 Withdrawn
71335264 Withdrawn
71335466 Withdrawn

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
K242375 2024-10-07
K232667 2023-10-27
K220959 2022-08-18
K211176 2022-07-01
K211330 2022-01-19
K191002 2019-10-31
K190847 2019-10-25
K182109 2018-11-16
K181366 2018-09-24
K171934 2017-11-30
K171073 2017-11-21
K172684 2017-10-03
K150790 2015-11-16
K123012 2012-10-24
K122244 2012-08-23
K110135 2011-10-14
K103256 2011-01-31
K092098 2010-01-22
K081566 2008-08-21
K072817 2008-05-15
K080625 2008-05-08
K072417 2008-01-10
K071160 2007-10-05
K060630 2006-06-14
K022902 2002-10-02
K022556 2002-08-28
K012787 2002-03-15
K013658 2001-12-05
K002747 2000-12-15
K991026 1999-10-22
K991485 1999-07-12
K983834 1999-02-24

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
2019-02-19 Class II Packaging process control Complaints were received indicating that the outer label incorrectly identified the product as size “1” instead of “-1”. The product contained within the package is size “-1” 58 units 2021-05-21
2019-02-19 Class II Packaging process control Complaints were received indicating that the outer label incorrectly identified the product as size “1” instead of “-1”. The product contained within the package is size “-1” 9 units 2021-05-21
2013-11-25 Class II Other One batch of the Reflection(TM) Polyethylene Acetabular Liners may be out of tolerance causing the liner not to fully seat into the shell. 38 units 2017-02-01
2008-11-21 Not classified Process control Liners measuring 28 mm ID and were mismarked as 32 mm. 19 units 2011-11-21

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