Reflection

Reflection Interfit Acetabular Shell Multi Hole Size 70MM

Registry build 21.09.26
5manufacturers in China registered for this device type
89catalogue numbers in this listing
9510(k) clearances naming this product code
9recalls on this code

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (2), Zhejiang (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MBL
Manufacturer City Province Registered as Device types
MicroPort Orthopedics Global Supply Center Limited Shanghai Shanghai Contract manufacturer 82
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
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106

Record

Regulatory record for Reflection
Listed by Smith & Nephew, Inc., United States
FDA product code MBL
Device type Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous
Device class Class 2
Regulation 21 CFR 888.3358
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K211176
Record published 2015-08-30
Record revised 2025-07-31 (version 9)

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 2016-01-10

Catalogue Numbers

Catalogue numbers for Reflection
Catalogue number Size Status
71336446 In distribution
71335070 In distribution
71334160 In distribution
71335050 In distribution
71336466 In distribution
71336458 In distribution
71336054 In distribution
71336362 In distribution
71336342 In distribution
71334154 In distribution
71334068 In distribution
71336450 In distribution
71336358 In distribution
71334146 In distribution
71334162 In distribution
71334042 In distribution
71335068 In distribution
71336044 In distribution
71335062 In distribution
71334066 In distribution
71336448 In distribution
71334046 In distribution
71334060 In distribution
71336056 In distribution
71335064 In distribution
71336050 In distribution
71336456 In distribution
71335074 In distribution
71336068 In distribution
71336464 In distribution
71335056 In distribution
71336346 In distribution
71336440 In distribution
71334064 In distribution
71336356 In distribution
71336444 In distribution
71336344 In distribution
71336462 In distribution
71334044 In distribution
71336042 In distribution
71334052 In distribution
71336046 In distribution
71335076 In distribution
71336048 In distribution
71335054 In distribution
71336454 In distribution
71334062 In distribution
71330001 In distribution
71336460 In distribution
71336468 In distribution
71336350 In distribution
71334056 In distribution
71336062 In distribution
71336354 In distribution
71336060 In distribution
71334150 In distribution
71334152 In distribution
71336366 In distribution
71336442 In distribution
71335072 In distribution
71334156 In distribution
71336340 In distribution
71334164 In distribution
71336500 In distribution
71335066 In distribution
71336352 In distribution
71335058 In distribution
71336364 In distribution
71335052 In distribution
71334158 In distribution
71336348 In distribution
71334148 In distribution
71334048 In distribution
71336064 In distribution
71336066 In distribution
71334054 In distribution
71334058 In distribution
71336360 In distribution
71335060 In distribution
71336058 In distribution
71336452 In distribution
71334050 In distribution
71336052 In distribution
71336368 In distribution
71932023 Withdrawn
71932024 Withdrawn
71932025 Withdrawn
71932026 Withdrawn
71932022 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
R3 Smith & Nephew, Inc. 177
Instrument Howmedica Osteonics Corp 100
Profemur® Microport Orthopedics Inc. 53
Delta Limacorporate 44
Onvoy Globus Medical, Inc. 40
Restoration Howmedica Osteonics Corp 39
Dynasty Microport Orthopedics Inc. 28
Delta Liners & Accessories Limacorporate 27
R3, Stiktite Smith & Nephew, Inc. 26
Biolox Delta Limacorporate 19
Tri-plus Ortho Development Corp. 16
Trident Howmedica Osteonics Corp 15

Showing 12 of 96. All products under Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K201701 2020-10-06
K182535 2018-11-19
K161233 2016-12-14
K113848 2012-04-27
K102370 2011-01-19
K093363 2010-01-26
K092386 2009-11-03
K070756 2007-06-06
K061253 2006-05-31

Recalls Naming This Product

7 recalls name this product by its own identifiers, 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 2020-04-22 Class II Process control A manufacturing error resulted in out of specification R3 Acetabular Shells 1267 devices
Smith & Nephew, Inc. 510(k) number 2020-04-22 Class II Process control A manufacturing error resulted in out of specification R3 Acetabular Shells 1450 devices
Smith & Nephew, Inc. 510(k) number 2020-04-22 Class II Process control A manufacturing error resulted in out of specification R3 Acetabular Shells 6468 devices
Smith & Nephew, Inc. 510(k) number 2020-04-22 Class II Process control A manufacturing error resulted in out of specification R3 Acetabular Shells 4172 devices
Smith & Nephew, Inc. 510(k) number 2020-04-22 Class II Process control A manufacturing error resulted in out of specification R3 Acetabular Shells 1766 devices
Smith & Nephew, Inc. 510(k) number 2020-04-22 Class II Process control A manufacturing error resulted in out of specification R3 Acetabular Shells 58 devices
Smith & Nephew, Inc. 510(k) number 2014-01-23 Class II Under Investigation by firm Inner spherical radius of the shell is undersized. 10 units 2016-11-15

Recalls

2 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
2013-05-29 Class II Packaging process control One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a 62 mm 20o liner and one batch of 62 mm 20o R3 XLPE liner may be laser etched and packaged as a 60 mm 20o liner. 53 units 2016-03-22
2013-05-29 Class II Packaging process control One batch of 60 mm 20o R3 XLPE liner may be laser etched and packaged as a 62 mm 20o liner and one batch of 62 mm 20o R3 XLPE liner may be laser etched and packaged as a 60 mm 20o liner. 53 units 2016-03-22

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