RHS – Radial Prosthesis

7 catalogue numbers from DTJ308, listed by Tornier Inc., United States, under Prosthesis, Elbow, Semi-Constrained, Cemented. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
7catalogue numbers in this listing
9510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Shanghai (2), Jiangsu (1).

Chinese manufacturers registered for FDA product code JDB
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34

Record

Regulatory record for RHS – Radial Prosthesis
Listed by Tornier Inc., United States
FDA product code JDB
Device type Prosthesis, Elbow, Semi-Constrained, Cemented
Device class Class 2
Regulation 21 CFR 888.3160
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-10-16
Record revised 2025-09-18 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries expiry date, manufacturing date, serial number
Sizes Outer diameter 6 to 20 mm

Catalogue Numbers

Catalogue numbers for RHS – Radial Prosthesis
Catalogue number Size Status
DTJ308 Outer Diameter 8 mm In distribution
DTJ106 Outer Diameter 6.5 mm In distribution
DTJ302 Outer Diameter 20 mm In distribution
DTJ317 Outer Diameter 7 mm In distribution
DTJ307 Outer Diameter 7 mm In distribution
DTJ310 Outer Diameter 10 mm In distribution
DTJ316 Outer Diameter 6 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Tema Elbow Limacorporate 90
Rhead Stryker GmbH 46
Latitude EV™ Tornier Inc. 33
Latitude™ – Elbow Tornier Inc. 22
UNI-Elbow Stryker GmbH 20
Tema Elbow System Limacorporate 9
Sorbie Questor ™ Wright Medical Technology, Inc. 9
AMK Depuy Orthopaedics, Inc. 8
AML TRI-Lock Depuy Orthopaedics, Inc. 2
Acclaim Depuy Orthopaedics, Inc. 2
Elite Depuy Intl., Ltd. 1
Latitude Tornier Inc. 1

Showing 12 of 18. All products under Prosthesis, Elbow, Semi-Constrained, Cemented

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K193247 2020-08-05
K182461 2018-12-27
K171010 2017-08-31
K100562 2010-06-29
K070787 2007-08-24
K060438 2006-04-18
K050848 2005-07-14
K031218 2003-05-16
K011567 2001-06-19

Recalls

1 of these is 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
2025-03-03 Class II Under Investigation by firm A specific lot of Latitude Humeral Trial Stems has the incorrect direct part marking.
” Laser Marked: 9030103, Humeral Stem Trial 150mm Large / Right, Yellow color indicator (incorrect)
” Device Actually: 9030092, Humeral Stem Trial 150mm M
5 units
2011-06-23 Not classified Process change control Tornier has discovered that some models of the Tornier latitude Elbow Prosthesis (Small and Medium Humeral stems) were manufactured with a humeral screw that may not function as designed. 3 2012-07-17

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