DCwire™

The filing describes DCwire as a single-use micro-guidewire with a shapeable tip for intravascular access and positioning or exchange of interventional devices. Its stated use includes…

Registry build 21.09.26

The filing describes DCwire as a single-use micro-guidewire with a shapeable tip for intravascular access and positioning or exchange of interventional devices.

Its stated use includes general intravascular access in neuro and peripheral vasculature, including selective introduction and positioning of catheters.

Design and Supplied Accessories

The device has Soft, Standard and Support stiffness profiles. The filing also identifies an introducer and a torque device as supplied accessories. The guidewire can be torqued to help navigate through the vasculature.

5manufacturers in China registered for this device type
8catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (2), Zhejiang (1), Beijing (1).

Chinese manufacturers registered for FDA product code MOF
Manufacturer City Province Registered as Device types
Terumo Medical Products (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Suzhou Zenith Vascular Scitech Limited Suzhou Jiangsu Manufacturer 6
Shanghai Achieva Medical Suzhou Co., Ltd. Suzhou Jiangsu Manufacturer 2
Deepintec Scientific Co., Ltd. Beijing Beijing Manufacturer 2
Enlight Medical Technologies (Shenzhen) Co., Ltd. Shenzhen Guangdong Manufacturer 1

Record

Regulatory record for DCwire™
Listed by Shanghai Achieva Medical Suzhou Co., Ltd., China
FDA product code MOF
Device type Guide, Wire, Catheter, Neurovasculature
Device class Class 2
Regulation 21 CFR 870.1330
Establishment Manufacturer
510(k) K252122
Record published 2026-07-03

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for DCwire™
Catalogue number Size Status
FG62001022 In distribution
FG62001433 In distribution
FG62001422 In distribution
FG62001023 In distribution
FG62001423 In distribution
FG62001412 In distribution
FG62001432 In distribution
FG62001413 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Willow 14 Guidewire Arbor Endovascular 22
Cypress 14 Guidewire Arbor Endovascular 9
Aristotle Scientia Vascular 8
Synchro Select Stryker GmbH 6
Chikai Nexus 014 Asahi Intecc Co., Ltd. 6
Hybrid Guidewire Balt USA, LLC 5
Chikai Asahi Intecc Co., Ltd. 4
Volo Scientia Vascular 4
Chikai black Asahi Intecc Co., Ltd. 4
Chikai Nexus petit Asahi Intecc Co., Ltd. 3
Agility Cerenovus, Inc. 3
Traxcess MicroVention, Inc. 3

Showing 12 of 42. All products under Guide, Wire, Catheter, Neurovasculature

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252122 2026-03-16

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