Stride Unicondylar Knee

STRIDE Tibial Insert Implant SIZE B, 10 mm

Registry build 21.09.26
6manufacturers in China registered for this device type
55catalogue numbers in this listing
1510(k) clearance

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 Stride Unicondylar Knee
Listed by Blue Belt Technologies, 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 Manufacturer
Record published 2015-09-24
Record revised 2018-03-29 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Distribution end date 2016-12-16

Catalogue Numbers

Catalogue numbers for Stride Unicondylar Knee
Catalogue number Size Status
110037 Withdrawn
110048 Withdrawn
110047 Withdrawn
110071 Withdrawn
110049 Withdrawn
110077 Withdrawn
110030 Withdrawn
110075 Withdrawn
110050 Withdrawn
110029 Withdrawn
110054 Withdrawn
110056 Withdrawn
110065 Withdrawn
110043 Withdrawn
110053 Withdrawn
110024 Withdrawn
110073 Withdrawn
110040 Withdrawn
110041 Withdrawn
110061 Withdrawn
110035 Withdrawn
110064 Withdrawn
110039 Withdrawn
110057 Withdrawn
110045 Withdrawn
110060 Withdrawn
110028 Withdrawn
110031 Withdrawn
110038 Withdrawn
110069 Withdrawn
110046 Withdrawn
110027 Withdrawn
110067 Withdrawn
110078 Withdrawn
110025 Withdrawn
110072 Withdrawn
110068 Withdrawn
110023 Withdrawn
110066 Withdrawn
110074 Withdrawn
110070 Withdrawn
110044 Withdrawn
110034 Withdrawn
110055 Withdrawn
110042 Withdrawn
110063 Withdrawn
110032 Withdrawn
110059 Withdrawn
110026 Withdrawn
110076 Withdrawn
110033 Withdrawn
110052 Withdrawn
110051 Withdrawn
110062 Withdrawn
110058 Withdrawn

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
K123380 2013-05-31

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