NVM5

NVM5 Connector Adapter/Needle Electrodes

Registry build 21.09.26
3manufacturers in China registered for this device type
11catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shandong (1), Shaanxi (1), Guangdong (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GWF
Manufacturer City Province Registered as Device types
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Xian Friendship Medical Electronics Co., Ltd. Xi’An Shaanxi Contract manufacturer 10
Shenzhen Launch Electrical Co., Ltd. Shenzhen Guangdong Contract manufacturer 8

Record

Regulatory record for NVM5
Listed by Nuvasive, Inc., United States
FDA product code GWF
Device type Stimulator, Electrical, Evoked Response
Device class Class 2
Regulation 21 CFR 882.1870
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K162313
Record published 2023-04-13
Record revised 2025-06-11 (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
Supplied as a kit Yes
Label carries lot or batch number, expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for NVM5
Catalogue number Size Status
1764188 In distribution
2021000 In distribution
1582845 In distribution
1017007 In distribution
2022022 In distribution
2010000 In distribution
1581268 In distribution
1566750 In distribution
1025906 In distribution
1581266 In distribution
2010400 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Stimulator, Electrical, Evoked Response Inomed Medizintechnik Gmbh 170
Alpine BioMed Alpine Biomed Aps 132
Natus Natus Neurology Incorporated 98
Keypoint Natus Manufacturing Limited 44
Stimulator, Electrical, Evoked Response Nihon Kohden America, Inc. 41
Stimulator, Electrical, Evoked Response Nihon Kohden Corp. 38
Powerease™ Instruments Medtronic Sofamor Danek, Inc. 36
Stimulator, Electrical, Evoked Response Stryker Leibinger Gmbh & Co. KG 29
Natus Xltek 27
Isis Inomed Medizintechnik Gmbh 26
Xltek Xltek 24
Natus Neurology Natus Neurology Incorporated 20

Showing 12 of 121. All products under Stimulator, Electrical, Evoked Response

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K094054 2010-05-14
K090298 2009-06-08
K072343 2007-10-29
K062765 2007-01-24
K051384 2005-07-11

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of NVM5
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Nuvasive, Inc. 510(k) number 2020-06-10 Class II Under Investigation by firm The NVM5 EMG Module kit intended for intraoperative neurophysiologic monitoring during spinal surgery contains incorrect component, part number 1715945, SSEP harness instead of the the correct part number 1747065, NVM5 Harness, Gen 3.5 EM. 23 2021-03-22

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