MicroPlex Helical Soft

56 catalogue numbers from 100406HC-S-V, listed by MicroVention, Inc., United States, under Device, Vascular, For Promoting Embolization. 6 manufacturers in China are registered for this product code.

Registry build 21.09.26
6manufacturers in China registered for this device type
56catalogue numbers in this listing
18510(k) clearances naming this product code
8recalls on this code

Who Else Makes It

Concentrated in Jiangsu (4), Guangdong (1), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code KRD
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Canyon Medical Inc. Nanjing Jiangsu Manufacturer 4
Suzhou Hengrui Hongyuan Medical Co., Ltd. Suzhou Jiangsu Manufacturer 3
Microport Neurotech (Shanghai) Co., Ltd. Shanghai Shanghai Manufacturer 2
Suzhou Haowei Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 1

Record

Regulatory record for MicroPlex Helical Soft
Listed by MicroVention, Inc., United States
FDA product code KRD
Device type Device, Vascular, For Promoting Embolization
Device class Class 2
Regulation 21 CFR 870.3300
Establishment Specification developer, Repacker / relabeller, Manufacturer, Exporter
Record published 2015-12-29
Record revised 2026-04-28 (version 7)

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, manufacturing date
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for MicroPlex Helical Soft
Catalogue number Size Status
100406HC-S-V 4 mm x 6 cm In distribution
100306HC-S-V 3 mm x 6 cm In distribution
100203HCSR-S-V 2 mm x 3 cm In distribution
100203HC-S-V 2 mm x 3 cm In distribution
100304HCSR-S-V 3 mm x 4 cm In distribution
100304HCSR-S-V-A1 3 mm x 4 cm In distribution
100310HC-S-V 3 mm x 10 cm In distribution
100208HCSR-S-V-A1 2 mm x 8 cm In distribution
100408HC-S-V 4 mm x 8 cm In distribution
100410HCSR-S-V 4 mm x 10 cm In distribution
100204HC-S-V 2 mm x 4 cm In distribution
100308HC-S-V-A1 3 mm x 8 cm In distribution
100308HCSR-S-V 3 mm x 8 cm In distribution
100310HCSR-S-V-A1 3 mm x 10 cm In distribution
100404HCSR-S-V-A1 4 mm x 4 cm In distribution
100303HC-S-V 3 mm x 3 cm In distribution
100404HC-S-V 4 mm x 4 cm In distribution
100206HCSR-S-V 2 mm x 6 cm In distribution
100306HCSR-S-V 3 mm x 6 cm In distribution
100408HC-S-V-A1 4 mm x 8 cm In distribution
100208HCSR-S-V 2 mm x 8 cm In distribution
100406HCSR-S-V-A1 4 mm x 6 cm In distribution
100408HCSR-S-V 4 mm x 8 cm In distribution
100303HC-S-V-A1 3 mm x 3 cm In distribution
100410HC-S-V 4 mm x 10 cm In distribution
100304HC-S-V-A1 3 mm x 4 cm In distribution
100208HC-S-V-A1 2 mm x 8 cm In distribution
100310HC-S-V-A1 3 mm x 10 cm In distribution
100303HCSR-S-V 3 mm x 3 cm In distribution
100408HCSR-S-V-A1 4 mm x 8 cm In distribution
100410HC-S-V-A1 4 mm x 10 cm In distribution
100206HC-S-V 2 mm x 6 cm In distribution
100206HC-S-V-A1 2 mm x 6 cm In distribution
100304HC-S-V 3 mm x 4 cm In distribution
100202HC-S-V 2 mm x 2 cm In distribution
100208HC-S-V 2 mm x 8 cm In distribution
100308HC-S-V 3 mm x 8 cm In distribution
100303HCSR-S-V-A1 3 mm x 3 cm In distribution
100204HCSR-S-V-A1 2 mm x 4 cm In distribution
100202HCSR-S-V 2 mm x 2 cm In distribution
100204HCSR-S-V 2 mm x 4 cm In distribution
100308HCSR-S-V-A1 3 mm x 8 cm In distribution
100203HC-S-V-A1 2 mm x 3 cm In distribution
100404HC-S-V-A1 4 mm x 4 cm In distribution
100204HC-S-V-A1 2 mm x 4 cm In distribution
100306HCSR-S-V-A1 3 mm x 6 cm In distribution
100203HCSR-S-V-A1 2 mm x 3 cm In distribution
100410HCSR-S-V-A1 4 mm x 10 cm In distribution
100404HCSR-S-V 4 mm x 4 cm In distribution
100202HCSR-S-V-A1 2 mm x 2 cm In distribution
100202HC-S-V-A1 2 mm x 2 cm In distribution
100406HCSR-S-V 4 mm x 6 cm In distribution
100206HCSR-S-V-A1 2 mm x 6 cm In distribution
100306HC-S-V-A1 3 mm x 6 cm In distribution
100310HCSR-S-V 3 mm x 10 cm In distribution
100406HC-S-V-A1 4 mm x 6 cm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Prestige Coil System Balt USA, LLC 339
Axium™ Detachable Coil System Micro Therapeutics, Inc. 279
Optima Coil System Balt USA, LLC 255
AxiumTM Micro Therapeutics, Inc. 255
Avenir Shanghai Wallaby Medical Technologies Co., Inc. 184
MReye Cook Incorporated 167
Axium™ Prime Detachable Coil System Micro Therapeutics, Inc. 162
Nester Cook Incorporated 160
Axium Micro Therapeutics, Inc. 146
ConcertoTM Micro Therapeutics, Inc. 133
Tornado Cook Incorporated 111
V-Trak MicroVention, Inc. 105

Showing 12 of 158. All products under Device, Vascular, For Promoting Embolization

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K223050 2022-12-21
K191680 2020-03-20
K162524 2017-03-03
K150870 2015-12-21
K151358 2015-09-25
K150958 2015-09-17
K133626 2013-12-20
K132083 2013-10-28
K130577 2013-06-17
K122543 2012-11-28
K123384 2012-11-28
K122316 2012-08-29
K120630 2012-03-28
K111307 2011-06-15
K102365 2010-11-18
K093002 2009-10-28
K091882 2009-07-08
K071939 2008-01-11

Recalls

8 of these are Class II. 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
2025-05-29 Class II Device Design Drug Elutable Microspheres have a smaller actual average diameter that is not within specification, which may lead to inability to reach the desired treatment location (non-targeted embolization), additional procedure/treatment required, bl 1451
2023-08-24 Class II Process control Peripheral coil system detachable has a potential of unsealed pouch packaging. 14
2019-11-24 Class II Other The devices may be missing the implant coil. 392 units 2021-04-20
2019-11-24 Class II Other The devices may be missing the implant coil. 1,187 units 2021-04-20
2019-11-24 Class II Other The devices may be missing the implant coil. 107 units 2021-04-20
2019-11-24 Class II Other The devices may be missing the implant coil. 19 units 2021-04-20
2019-11-24 Class II Other The devices may be missing the implant coil. 3,881 units 2021-04-20
2019-11-24 Class II Other The devices may be missing the implant coil. 445 units 2021-04-20

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P780011 1988-01-29 MINI BALLOON Bd Becton Dickinson Vacutainer Systems Preanalytic

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