swiftMATCH Coil, Soft

swiftMATCH Coil, Soft, 5mm x 10cm

Registry build 21.09.26
5manufacturers in China registered for this device type
5catalogue numbers in this listing
10510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (2), Guangdong (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 HCG
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
Shanghai Wallaby Medical Technologies Co., Inc. Shanghai Shanghai Contract manufacturer 5
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Microport Neurotech (Shanghai) Co., Ltd. Shanghai Shanghai Manufacturer 2

Record

Regulatory record for swiftMATCH Coil, Soft
Listed by Penumbra Inc., United States
FDA product code HCG
Device type Device, Neurovascular Embolization
Device class Class 2
Regulation 21 CFR 882.5950
Establishment Manufacturer, Exporter
510(k) K230284
Record published 2026-01-26

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for swiftMATCH Coil, Soft
Catalogue number Size Status
400SWSFT510-A In distribution
400SWSFT306-A In distribution
400SWSFT410-A In distribution
400SWSFT406-A In distribution
400SWSFT515-A In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Optima Coil System Balt USA, LLC 307
Penumbra Coil 400 Penumbra Inc. 268
Smart Coil Penumbra Inc. 238
Axium™ Detachable Coil System Micro Therapeutics, Inc. 234
Numen Microport Neurotech (Shanghai) Co., Ltd. 223
Axium™ Prime Detachable Coil System Micro Therapeutics, Inc. 141
Barricade Coil System Balt USA, LLC 137
Numen Helia Microport Neurotech (Shanghai) Co., Ltd. 129
V-Trak MicroVention, Inc. 106
HydroSoft Helical MicroVention, Inc. 94
AxiumTM Micro Therapeutics, Inc. 89
LP Coil System Penumbra Inc. 77

Showing 12 of 99. All products under Device, Neurovascular Embolization

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K230284 2023-10-25
K192955 2019-11-20
K173614 2018-04-17
K170852 2017-07-19
K160832 2016-04-20
K151572 2015-07-10
K143218 2015-03-18
K141134 2014-07-03
K120330 2012-04-02
K103305 2011-01-26

Recalls

The FDA has not published a severity grade for these. 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
2011-03-04 Not classified Process change control The diameter of a component of the device is out of tolerance specification; the Delivery Pusher pull wire which secures the coil in place can prolapse and allow premature detachment of the coil. 2082 2011-06-06

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