Latitude EV™

Humeral Stem - Coated

Registry build 21.09.26
3manufacturers in China registered for this device type
33catalogue 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 Latitude EV™
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 2019-05-08
Record revised 2025-12-16 (version 6)

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
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date, serial number
Sizes Length 30 to 200 mm; outer diameter 6 to 20 mm

Catalogue Numbers

Catalogue numbers for Latitude EV™
Catalogue number Size Status
0830818 Length 45 mm In distribution
0030313 Size SMALL In distribution
0030020 Size SMALL In distribution
9039005 Outer Diameter 10 mm In distribution
0030522 Size LARGE In distribution
0030502 Length 83 mm In distribution
0030302 Length 72 mm In distribution
0030402 Size MEDIUM In distribution
9030346 Size MEDIUM In distribution
0030221 Size LARGE In distribution
0030513 Length 150 mm In distribution
0030130 Size MEDIUM In distribution
0030322 Length 200 mm In distribution
0830819 Outer Diameter 8 mm In distribution
0030323 Size SMALL In distribution
0030011 Length 41 mm In distribution
0030503 Size LARGE In distribution
0030240 Size LARGE In distribution
9030356 Size LARGE+ In distribution
0030110 Length 47 mm In distribution
0030230 Size LARGE In distribution
0830822 Size SMALL In distribution
0030423 Size MEDIUM In distribution
0030422 Size MEDIUM In distribution
0030303 Size SMALL In distribution
0030141 Size MEDIUM In distribution
0030031 Size SMALL In distribution
9030341 Size SMALL In distribution
0830820 Outer Diameter 8 mm In distribution
0030720 Size LARGE In distribution
0830823 Outer Diameter 20 mm In distribution
0030701 Size SMALL In distribution
9030351 Size LARGE 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™ – 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
RHS – Radial Prosthesis Tornier Inc. 7
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