Nexdrive™

MI-2000 NEXDRIVE™ Micropositioning Drive

Registry build 21.09.26
5manufacturers in China registered for this device type
2catalogue numbers in this listing
6510(k) clearances naming this product code
24recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (1), Shandong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HAW
Manufacturer City Province Registered as Device types
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Sinovation (Beijing) Medical Technology Co., Ltd. Beijing Beijing Manufacturer 1

Record

Regulatory record for Nexdrive™
Listed by FHC, Inc., United States
FDA product code HAW
Device type Neurological Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
Establishment Complaint-file establishment, Manufacturer
510(k) K022100
Record published 2025-04-30

Specifications

Specifications
MRI safety MR Unsafe
Sterilisation Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment temperature -34 to 57 °C

Catalogue Numbers

Catalogue numbers for Nexdrive™
Catalogue number Size Status
MI-2000-00871 In distribution
MI-2000-00772 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Neurological Stereotaxic Instrument Medtronic Navigation, Inc. 844
PMT Corporation – Stereotactic PMT Corp. 255
Leksell Stereotactic System Elekta Instrument AB 199
Neurological Stereotaxic Instrument Inomed Medizintechnik Gmbh 146
Neurological Stereotaxic Instrument Stryker Leibinger Gmbh & Co. KG 125
Geniant Cranial KOH Young Technology Inc. 113
CRW® Integra Lifesciences Corporation 107
Leksell Stereotactic System Elekta Solutions AB 93
microTargeting™ Insertion Tube with Stylet FHC, Inc. 60
Leksell Stereotactic System Neurosurgical Instruments Elekta Instrument AB 58
Leksell Vantage Stereotactic System Elekta Instrument AB 53
Stealth Autoguide™ System Medtronic Navigation, Inc. 50

Showing 12 of 1,137. All products under Neurological Stereotaxic Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K121950 2012-07-26
K092192 2010-02-12
K092562 2009-09-18
K011775 2001-08-30
K011992 2001-08-14
K003776 2001-02-23

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Nexdrive™
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Medtronic Neuromodulation 510(k) number 2014-06-11 Class II Nonconforming Material/Component Potential for misalignment of the Z-stage scale. Using one of these devices for a procedure could result in the microelectrode being inserted to an incorrect target depth. 300 EXPANDED 10/02/2014 130 devices 2015-01-22
Medtronic Image Guided Neurologics, Inc. 510(k) number 2007-10-04 Not classified Package design/selection Sterilty (package integrity) Compromised: Some failures were for damage to the outer pouch, while another set of failures were for the seals on this pouch. The seal between the inner tray and lid has not been compromised and the contents 385 2012-07-13

Recalls

1 of these is Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. 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
2024-10-04 Class I Process change control A complaint was received (MDR 3002250546-2024-00003) prompting an investigation. The investigation revealed a schematic for a spacer tube which is too long relative to the size of other components was included in the build order for Lot 244 8 packs of 5ea (40 total)
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2010-03-30 Not classified Device Design Fixation thumbscrew on the DBS depth stop adapter may be overtightened and damage the implantable lead. 18 units 2015-02-25
2010-03-30 Not classified Device Design Fixation thumbscrew on the DBS depth stop adapter
may be overtightened and damage the implantable lead.
37 2015-02-25
2010-03-30 Not classified Device Design Fixation thumbscrew on the DBS depth stop adapter
may be overtightened and damage the implantable lead.
7 2015-02-25
2010-03-30 Not classified Device Design Fixation thumbscrew on the DBS depth stop adapter
may be overtightened and damage the implantable lead.
1 2015-02-25
2008-10-08 Not classified Process control Measuring fixture is incorrectly graduated. 5 units 2012-05-02
2005-10-31 Not classified Other Power Assist microTargeting System may advance beyond intended target 70 units 2006-06-07
2005-10-31 Not classified Other Power Assist microTargeting System may advance beyond intended target 230 units 2006-06-07
2005-03-14 Not classified Other Potential for non-sterile pin to contaminate sterile field 169 units 2008-07-08

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