SL-Plus

SL-Plus MIA Modular Neck FOR Detachable Rasp Standard 01-0

Registry build 21.09.26
14manufacturers in China registered for this device type
37catalogue numbers in this listing
1510(k) clearance
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (7), 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 KWY
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
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
Lincotek (Wuxi) Co., Ltd. Wuxi Jiangsu Contract manufacturer 7
b-ONE Medical (Beijing) Co., Ltd. Beijing Beijing 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

Showing 12 of 14. All 14 manufacturers in China registered for Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

Record

Regulatory record for SL-Plus
Listed by Smith & Nephew, Inc., United States
FDA product code KWY
Device type Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented
Device class Class 2
Regulation 21 CFR 888.3390
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K123598
Record published 2015-11-25
Record revised 2024-09-11 (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: : –

Catalogue Numbers

Catalogue numbers for SL-Plus
Catalogue number Size Status
75007310 In distribution
75002715 In distribution
75004604 In distribution
75002758 In distribution
75002320 In distribution
75004494 In distribution
75002719 In distribution
75002748 In distribution
75002769 In distribution
75002319 In distribution
75007303 In distribution
75002711 In distribution
75002756 In distribution
75002717 In distribution
75002750 In distribution
75002703 In distribution
75002766 In distribution
75002707 In distribution
75002695 In distribution
75002709 In distribution
75002752 In distribution
75002764 In distribution
75002762 In distribution
75004490 In distribution
75002713 In distribution
75002699 In distribution
75007306 In distribution
75002697 In distribution
75002701 In distribution
75007300 In distribution
75002770 In distribution
75002714 In distribution
75002705 In distribution
75002768 In distribution
75007309 In distribution
75002760 In distribution
75004603 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Resolve Modular Revision Hip Stem United Orthopedic Corp. 196
Corin Bipolar Prosthesis Corin Limited 182
Consensus® Hip System Consensus Orthopedics, Inc. 177
Consensus Hip System Shalby Advanced Technologies, Inc. 177
Instrument Howmedica Osteonics Corp 130
Bencox Hip System Corentec Co., Ltd. 126
United Hip System, U2 Bipolar Implant United Orthopedic Corp. 123
MultiPolar® Zimmer, Inc. 100
Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented Zimmer, Inc. 96
Fitmore® Hip Stem Zimmer, Inc. 75
Arcos® Modular Revision System Biomet Orthopedics 67
Acumatch L-Series Exactech, Inc. 67

Showing 12 of 352. All products under Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K023743 2003-01-23

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of SL-Plus
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Smith & Nephew, Inc. 510(k) number 2024-10-15 Class II Under Investigation by firm The Bipolar assembly contains an oversized Retainer Ring. 21 devices
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

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
2016-08-29 Class II Process control Some Bipolar shells were manufactured with an out of specification retainer groove. 5806 units 2019-08-16
2016-08-29 Class II Process control Some Bipolar shells were manufactured with an out of specification retainer groove. 2352 units 2019-08-16

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