Engage

Engage Porous Coated Femoral Size 1-RIGHT Medial

Registry build 21.09.26
6manufacturers in China registered for this device type
105catalogue numbers in this listing
13510(k) clearances naming this product code
40recalls on this code

Who Else Makes It

Concentrated in Zhejiang (2), Jiangsu (2), Shanghai (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 HSX
Manufacturer City Province Registered as Device types
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
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74

Record

Regulatory record for Engage
Listed by Smith & Nephew, Inc., United States
FDA product code HSX
Device type Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
Device class Class 2
Regulation 21 CFR 888.3520
Establishment Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K190439
Record published 2023-01-13
Record revised 2025-07-25 (version 3)

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: : –
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Engage
Catalogue number Size Status
1-50080-002 In distribution
1-50043-309 In distribution
1-10013-663 In distribution
1-50043-213 In distribution
1-50043-509 In distribution
1-50025-006 In distribution
1-50060-001 In distribution
1-51041-003 In distribution
1-10013-509 In distribution
1-10013-211 In distribution
1-10013-511 In distribution
1-10013-409 In distribution
1-51036-004 In distribution
1-50065-002 In distribution
1-10012-300 In distribution
1-50042-613 In distribution
1-50062-002 In distribution
1-10013-261 In distribution
1-10012-550 In distribution
1-50043-311 In distribution
1-10012-250 In distribution
1-51030-003 In distribution
1-10013-360 In distribution
1-10013-461 In distribution
1-50042-313 In distribution
1-50042-513 In distribution
1-50043-113 In distribution
1-10003-400 In distribution
1-50042-311 In distribution
1-10003-100 In distribution
1-10013-359 In distribution
1-10003-300 In distribution
1-10013-609 In distribution
1-10013-312 In distribution
1-51031-002 In distribution
1-10013-362 In distribution
1-51059-000 In distribution
1-50060-021 In distribution
1-10013-661 In distribution
1-50061-001 In distribution
1-50104-045 In distribution
1-10012-650 In distribution
1-10013-110 In distribution
1-10013-363 In distribution
1-51058-000 In distribution
1-50043-409 In distribution
1-50017-056 In distribution
1-50042-510 In distribution
1-50061-002 In distribution
1-10011-100 In distribution
1-50064-000 In distribution
1-50024-003 In distribution
1-50043-109 In distribution
1-51041-005 In distribution
1-10013-662 In distribution
1-50042-209 In distribution
1-51030-006 In distribution
1-50017-012 In distribution
1-50042-309 In distribution
1-50082-000 In distribution
1-10003-610 In distribution
1-10003-510 In distribution
1-10012-450 In distribution
1-50043-611 In distribution
1-50042-210 In distribution
1-10013-313 In distribution
1-50024-006 In distribution
1-51040-005 In distribution
1-50040-003 In distribution
1-50042-113 In distribution
1-50017-034 In distribution
1-50043-511 In distribution
1-50042-410 In distribution
1-10012-150 In distribution
1-50028-002 In distribution
1-10013-112 In distribution
1-10013-160 In distribution
1-10013-260 In distribution
1-10003-710 In distribution
1-10013-612 In distribution
1-50041-004 In distribution
1-50035-000 In distribution
1-10013-111 In distribution
1-51035-000 In distribution
1-10013-560 In distribution
1-50040-006 In distribution
1-10013-210 In distribution
1-51040-004 In distribution
1-50024-004 In distribution
1-50025-001 In distribution
1-10013-262 In distribution
1-51037-004 In distribution
1-51040-006 In distribution
1-10013-162 In distribution
1-50042-611 In distribution
1-51031-007 In distribution
1-50040-001 In distribution
1-50025-005 In distribution
1-10013-212 In distribution
1-10003-210 In distribution
1-50025-003 In distribution
1-50040-002 In distribution
1-10011-300 In distribution
1-10013-263 In distribution
1-50042-609 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Journey Smith & Nephew, Inc. 517
Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer Ortho Development Corp. 303
BKS® Uni Ortho Development Corp. 240
LinkSymphoKnee Waldemar Link GmbH & Co. KG 210
Moto Partial Knee System Medacta International SA 205
Arthrex® Arthrex, Inc. 199
Stride Smith & Nephew, Inc. 190
Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer Zimmer, Inc. 175
ZUK Smith & Nephew, Inc. 161
Tahoe Uni Knee System Shalby Advanced Technologies, Inc. 134
Moto Partial Knee System – Medial Medacta International SA 132
Journey II Smith & Nephew, Inc. 119

Showing 12 of 171. All products under Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242711 2024-10-30
K211512 2021-09-16
K191211 2019-07-25
K190085 2019-02-11
K160738 2016-06-15
K152315 2015-10-28
K113038 2012-01-05
K102069 2010-10-05
K100197 2010-02-19
K081351 2008-07-24
K073175 2007-12-20
K061779 2006-08-04
K061011 2006-07-11

Recalls Naming This Product

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

Recalls naming the identifiers of Engage
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Smith & Nephew, Inc. 510(k) number 2023-05-02 Class II Under Investigation by firm Recent complaint data indicates that the revision rate may be trending higher than corresponding similar
devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the st
1994 units
Smith & Nephew, Inc. 510(k) number 2023-05-02 Class II Under Investigation by firm Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the st 1596 units
Smith & Nephew, Inc. 510(k) number 2023-05-02 Class II Under Investigation by firm Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the st 2146 units
Smith & Nephew, Inc. 510(k) number 2023-05-02 Class II Under Investigation by firm Recent complaint data indicates that the revision rate may be trending higher than corresponding similar devices in global joint replacement registries. The data identifies a potential signal that the performance is an outlier versus the st 7531 units

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
2023-03-27 Class II Under Investigation by firm A mispack occurred during the manufacturing process, resulting in the box incorrectly containing JOURNEY II UNI Tibia Insert Medical Size 1-2 12MM instead of the JOURNEY II UNI Tibia Insert Medial Size 7-8 8MM. 12 units
2020-01-28 Class II Process design The spike rail was manufactured with an oversized thru-hole which could potentially cause the dowel pin to fall out and the device to disassemble. 195 units 2023-12-11
2020-01-28 Class II Process design The spike rail was manufactured with an oversized thru-hole which could potentially cause the dowel pin to fall out and the device to disassemble. 200 units 2023-12-11
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 58 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 859 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 904 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 941 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1421 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 353 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1150 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 71 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1004 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 704 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 56 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 628 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 849 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 817 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 60 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 57 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 960 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 838 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 379 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 863 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 895 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 734 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 89 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1064 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 813 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 721 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 97 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1283 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 69 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 952 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 713 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1324 units 2011-03-25
2009-01-23 Not classified Device Design The firm has received complaints of the base plates breaking in situ. If a breakage occurs, the broken baseplate must be revised and/or changed. If left unrevised a broken base could lead to instability and premature wear of the construct. 1015 units 2011-03-25

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