Armada

Armada Ti Tap, 5.5mm Extend Double Lead

Registry build 21.09.26
8manufacturers in China registered for this device type
67catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (2), Jiangsu (2), Guangdong (2). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code ETN
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Forefront Medical Technology (Jiangsu) Co., Ltd. Changzhou Jiangsu Contract manufacturer 14
Xian Friendship Medical Electronics Co., Ltd. Xi’An Shaanxi Contract manufacturer 10
Ningbo Shun YE Medical Company, Ltd. Cixi Ningbo Zhejiang Contract manufacturer 8
Shenzhen Launch Electrical Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Pine Moon Electronics Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Changzhou Emanmed Biotechnology Co., Ltd. Changzhou Jiangsu Contract manufacturer 4

Record

Regulatory record for Armada
Listed by Nuvasive, Inc., United States
FDA product code ETN
Device type Stimulator, Nerve
Device class Class 2
Regulation 21 CFR 874.1820
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K112709
Record published 2016-09-24
Record revised 2025-06-11 (version 7)

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

Catalogue Numbers

Catalogue numbers for Armada
Catalogue number Size Status
7559140 In distribution
7459275 In distribution
7459295 In distribution
7459855 In distribution
7559141 In distribution
7459107 In distribution
7453050 In distribution
7459146 In distribution
D7659014 In distribution
7459165 In distribution
7459005 In distribution
7453065 In distribution
7459006 In distribution
7459865 In distribution
7459125 In distribution
7453055 In distribution
7459955 In distribution
7559165 In distribution
7451107 In distribution
7459965 In distribution
7451014 In distribution
7559014 In distribution
7459945 In distribution
7459185 In distribution
D7459107 In distribution
7451089 In distribution
7459285 In distribution
7459140 In distribution
7453085 In distribution
7459845 In distribution
7559131 In distribution
7459003 In distribution
7453045 In distribution
7459145 In distribution
7559132 In distribution
7559175 In distribution
7459801 In distribution
7459088 In distribution
7453075 In distribution
7559135 In distribution
7459975 In distribution
7459148 In distribution
7459199 In distribution
7559185 In distribution
7459901 In distribution
7459255 In distribution
7559088 In distribution
7459014 In distribution
7459004 In distribution
7459150 In distribution
7451104 In distribution
7459175 In distribution
7459902 In distribution
7451090 In distribution
7559150 In distribution
7559155 In distribution
7459195 In distribution
7459155 In distribution
7459265 In distribution
D7459104 In distribution
7459104 In distribution
D7459014 In distribution
7451080 In distribution
7559145 In distribution
7459225 In distribution
7459875 In distribution
7453040 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ReLine Nuvasive, Inc. 226
Stimulator, Nerve Medtronic Xomed, Inc. 125
MaXcess Nuvasive, Inc. 95
Stimulator, Nerve Neurovision Medical Products, Inc. 47
Precept Nuvasive, Inc. 39
MAS Plif Nuvasive, Inc. 36
NIM Medtronic Xomed, Inc. 34
Nerveana® Neurovision Medical Products, Inc. 30
SpheRx Nuvasive, Inc. 30
IOM Stimulator Probes Spes Medica Srl 29
NVM5 Nuvasive, Inc. 25
NIM TriVantage® Medtronic Xomed, Inc. 25

Showing 12 of 119. All products under Stimulator, Nerve

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K112717 2012-04-13
K112718 2012-03-16
K111597 2011-10-13
K051718 2005-09-15
K040543 2004-04-01
K032083 2003-10-24

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