Expedium

EXPEDIUM SPINE SYSTEM SINGLE INLINE RODDED CONNECTOR 6.35 x 5.5-6.35X200mm

Registry build 21.09.26
14manufacturers in China registered for this device type
191catalogue numbers in this listing
10510(k) clearances naming this product code
8recalls on this code

Who Else Makes It

Concentrated in Jiangsu (5), Shanghai (3), Zhejiang (2). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KWQ
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14

Showing 12 of 14. All 14 manufacturers in China registered for Appliance, Fixation, Spinal Intervertebral Body

Record

Regulatory record for Expedium
Listed by Depuy Spine, Inc., United States
FDA product code KWQ
Device type Appliance, Fixation, Spinal Intervertebral Body
Device class Class 2
Regulation 21 CFR 888.3060
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K073364
Record published 2015-09-24
Record revised 2025-07-02 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2024-06-14

Catalogue Numbers

Catalogue numbers for Expedium
Catalogue number Size Status
187701004 In distribution
187703060 In distribution
186112560 In distribution
186112690 In distribution
187701008 In distribution
187702640 In distribution
186153360 In distribution
186154650R In distribution
187702655 In distribution
187702750 In distribution
186112022 In distribution
187701003 In distribution
187704013 In distribution
187703100 In distribution
186154330 In distribution
187703045 In distribution
186188670 In distribution
186132445 In distribution
186153180 In distribution
186272020 In distribution
187702742 In distribution
186102680 In distribution
187704017 In distribution
187703050 In distribution
187702735 In distribution
187701007 In distribution
187702532 In distribution
186100003 In distribution
187703090 In distribution
186102035 In distribution
186112440 In distribution
187702625 In distribution
179998300 In distribution
187703080 In distribution
187704014 In distribution
186161412 In distribution
187702745 In distribution
187702627 In distribution
186100005 In distribution
187704005 In distribution
186112050 In distribution
187703085 In distribution
186188635 In distribution
187702630 In distribution
186132522 In distribution
187703130 In distribution
186153380 In distribution
187701015 In distribution
187703110 In distribution
187702740 In distribution
188163600 In distribution
186188015 In distribution
186188450 In distribution
186152360 In distribution
186161460 In distribution
186152650L In distribution
187704015 In distribution
186142025 In distribution
186112015 In distribution
187702545 In distribution
187702527 In distribution
186102670 In distribution
187702645 In distribution
179798300 In distribution
186152430 In distribution
187702542 In distribution
187701005 In distribution
186132035 In distribution
186132440 In distribution
187702537 In distribution
187702647 In distribution
186132045 In distribution
186122025 In distribution
186172065 In distribution
187701010 In distribution
187702635 In distribution
186152740 In distribution
187701002 In distribution
186112699 In distribution
187704016 In distribution
187702642 In distribution
186188427 In distribution
186152640L In distribution
186154340 In distribution
186188665 In distribution
186153440 In distribution
186172945 In distribution
187703075 In distribution
187703055 In distribution
187702637 In distribution
186112425 In distribution
187703065 In distribution
186142430 In distribution
187702632 In distribution
187702660 In distribution
187704018 In distribution
187703070 In distribution
186112670 In distribution
186132027 In distribution
186132625 In distribution
186173945 In distribution
187703450 In distribution
186112030 In distribution
187703140 In distribution
187702525 In distribution
186100009 In distribution
187701009 In distribution
187702650 In distribution
187703095 In distribution
187701001 In distribution
187703120 In distribution
187701006 In distribution
186112570 In distribution
186132655 In distribution
186172155 In distribution
186153450 In distribution
186188520 In distribution
187702755 In distribution
187702530 In distribution
187703150 In distribution
187702535 In distribution
187702540 In distribution
186202535 Withdrawn
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186252640R Withdrawn
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188102845 Withdrawn
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186252140 Withdrawn
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186212520 Withdrawn
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186288425 Withdrawn
186252340 Withdrawn
188112655 Withdrawn
186252780 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ReLine Nuvasive, Inc. 2,998
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 2,568
Creo Globus Medical, Inc. 1,765
AccelFix Spinal Fixation System L&K Biomed Co., Ltd. 1,755
Ozark Cervical Plate System VB Spine LLC 1,460
Sirion Astura Medical 1,246
Apex Spine System Spinecraft LLC 1,187
AnyPlus Spinal Fixation System GS Medical Co., Ltd. 986
Astra Spine System Spinecraft LLC 970
Zavation Zavation 966
ACP Nuvasive, Inc. 918
Polaris™ 5.5 Spinal System Biomet Spine 877

Showing 12 of 855. All products under Appliance, Fixation, Spinal Intervertebral Body

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K100070 2010-02-04
K082273 2008-09-10
K080191 2008-04-02
K072546 2007-10-05
K070994 2007-05-09
K052546 2006-02-03
K052552 2005-10-13
K042544 2004-11-23
K041205 2004-08-17
K040655 2004-06-02

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 Expedium
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Depuy Spine, Inc. 510(k) number 2015-04-21 Class II Process design Device does not mate as intended. 183 devices 2018-10-03

Recalls

8 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
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 1 unit 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 14 units 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 6 units 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 9 units 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 12 units 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 9 units 2017-09-18
2016-10-12 Class II Under Investigation by firm SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws within the packaging. 21 units 2017-09-18
2015-11-20 Class II Device Design Manufacturing error within the Torque Handle may prohibit some handles from being able to fully assemble with the tightener shaft. The design of the inspection gage does not account for the additional shift length 16 devices 2017-07-03

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