Reflection

Reflection Xlpe 28MM Inner Diameter 0 Degree Lateralized +4MM 62-64MM Outer Diameter Size H

Registry build 21.09.26
13manufacturers in China registered for this device type
170catalogue numbers in this listing
8510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (3), Zhejiang (2). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JDI
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
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
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54

Showing 12 of 13. All 13 manufacturers in China registered for Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Record

Regulatory record for Reflection
Listed by Smith & Nephew, Inc., United States
FDA product code JDI
Device type Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
Device class Class 2
Regulation 21 CFR 888.3350
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K123598
Record published 2015-08-30
Record revised 2023-09-07 (version 9)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
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
71362672 In distribution
71333477 In distribution
71358035 In distribution
71333326 In distribution
71922898 In distribution
71358068 In distribution
71333413 In distribution
71362652 In distribution
71333314 In distribution
71358029 In distribution
71333453 In distribution
71362660 In distribution
71333377 In distribution
71333414 In distribution
71333488 In distribution
71333302 In distribution
71333487 In distribution
71333426 In distribution
71929753 In distribution
71333464 In distribution
71333474 In distribution
71333379 In distribution
71362256 In distribution
71333366 In distribution
71362239 In distribution
71333424 In distribution
71333429 In distribution
71362656 In distribution
71333354 In distribution
71333313 In distribution
71333363 In distribution
71929748 In distribution
71333350 In distribution
71333462 In distribution
71333312 In distribution
71358036 In distribution
71333367 In distribution
71333307 In distribution
71333402 In distribution
71333412 In distribution
71333318 In distribution
71333489 In distribution
71362268 In distribution
E0015496-1 In distribution
71333427 In distribution
71333389 In distribution
71358034 In distribution
71333353 In distribution
71333484 In distribution
71362648 In distribution
71333428 In distribution
71333416 In distribution
71333324 In distribution
71333338 In distribution
71333403 In distribution
71929755 In distribution
71333325 In distribution
71333336 In distribution
71333301 In distribution
71333374 In distribution
71333309 In distribution
71362264 In distribution
71333388 In distribution
71333378 In distribution
71358028 In distribution
71358026 In distribution
71333323 In distribution
71333452 In distribution
71333305 In distribution
71929752 In distribution
71333401 In distribution
71333467 In distribution
71333319 In distribution
71358023 In distribution
71333375 In distribution
71333352 In distribution
71333365 In distribution
71358003 In distribution
71362252 In distribution
71358008 In distribution
71333486 In distribution
71333479 In distribution
71358002 In distribution
71362260 In distribution
71333478 In distribution
71333300 In distribution
71333304 In distribution
71362671 In distribution
71333373 In distribution
71333438 In distribution
71333315 In distribution
71358065 In distribution
71362237 In distribution
71333450 In distribution
71333328 In distribution
71333456 In distribution
71333485 In distribution
71333451 In distribution
71358025 In distribution
71333417 In distribution
71358024 In distribution
71333476 In distribution
71358066 In distribution
71333316 In distribution
71358037 In distribution
71333327 In distribution
71929754 In distribution
71333358 In distribution
71333386 In distribution
71333407 In distribution
71333376 In distribution
71333339 In distribution
71333335 In distribution
71333329 In distribution
71362238 In distribution
71333436 In distribution
71333303 In distribution
71333387 In distribution
71333362 In distribution
71333425 In distribution
71358007 In distribution
71333406 In distribution
71333334 In distribution
71358005 In distribution
71358039 In distribution
71333437 In distribution
71362664 In distribution
71333400 In distribution
71333457 In distribution
71333466 In distribution
71362248 In distribution
71362272 In distribution
71358006 In distribution
71333351 In distribution
71333423 In distribution
71362635 In distribution
71362270 In distribution
71333384 In distribution
71333439 In distribution
71358004 In distribution
71333404 In distribution
71333337 In distribution
71929749 In distribution
71333473 In distribution
71333454 In distribution
71362670 In distribution
71333455 In distribution
71333415 In distribution
71333465 In distribution
71358027 In distribution
71333317 In distribution
71929750 In distribution
71333434 In distribution
71929751 In distribution
71358069 In distribution
71358001 In distribution
71333405 In distribution
71358067 In distribution
71358038 In distribution
71333308 In distribution
71362668 In distribution
71333385 In distribution
71333463 In distribution
71333435 In distribution
71333364 In distribution
71333475 In distribution
E0014440 Withdrawn
E0014440-1 Withdrawn
71922906 Withdrawn
71926509 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented Zimmer, Inc. 836
R3 Smith & Nephew, Inc. 497
UniSyn Hip System Shalby Advanced Technologies, Inc. 247
UniSyn® Hip System Consensus Orthopedics, Inc. 247
Instrument Howmedica Osteonics Corp 167
Echelon Smith & Nephew, Inc. 159
B-P Total HIP System Endotec, Inc. 151
ZCA® Zimmer, Inc. 149
Omnifit Howmedica Osteonics Corp 149
Ringloc HIP System Biomet Orthopedics 139
Profemur Microport Orthopedics Inc. 113
OSS™ Orthopedic Salvage System Biomet Orthopedics 98

Showing 12 of 444. All products under Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K240783 2024-10-21
K160923 2016-11-17
K123598 2013-06-28
K052792 2005-10-07
K030766 2003-07-25
K024340 2003-02-26
K022958 2002-10-02
K990369 1999-03-12

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 Reflection
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Smith & Nephew, Inc. 510(k) number 2016-11-16 Class II Process control The firm received complaints of cracks in the weld on the head of the mallet. In the reported cases, some of the lead beads and particles escaped from the mallet into the surgical wound. 4444 units 2019-08-19

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
2018-05-02 Class II Process control Three lots of Anthology HO Porous size 7 stems were manufactured with an undersized taper length. The device taper length was incorrectly manufactured as 0.393mm opposed to 0.442 mm. 13 units 2020-09-01
2009-01-23 Not classified Other Radius at the end of the taper of the femoral implant is smaller than specification. This error could result in the tapers not locking fully or properly on femoral stems or in causing impingement and/or increased wear debris. The deficienc 925 units 2012-02-07

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