Embold™ Fibered
24 catalogue numbers from M001394240200500, listed by Boston Scientific Corporation, United States, under Device, Vascular, For Promoting Embolization. 6 manufacturers in China are registered for this product 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.
| 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
| Listed by | Boston Scientific Corporation, 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, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2022-04-20 |
Specifications
| MRI safety | MR Conditional |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Sizes | Outer diameter 2 to 32 mm; length 4 to 60 cm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| M001394240200500 | Outer Diameter 20 mm | In distribution |
| M001394240100500 | Outer Diameter 10 mm | In distribution |
| M001394240050080 | Length 8 cm | In distribution |
| M001394240100300 | Outer Diameter 10 mm | In distribution |
| M001394240050150 | Outer Diameter 5 mm | In distribution |
| M001394240140500 | Outer Diameter 14 mm | In distribution |
| M001394240220600 | Outer Diameter 22 mm | In distribution |
| M001394240040150 | Outer Diameter 4 mm | In distribution |
| M001394240040080 | Outer Diameter 4 mm | In distribution |
| M001394240020060 | Outer Diameter 2 mm | In distribution |
| M001394240060200 | Outer Diameter 6 mm | In distribution |
| M001394240080200 | Length 20 cm | In distribution |
| M001394240020040 | Outer Diameter 2 mm | In distribution |
| M001394240320600 | Length 60 cm | In distribution |
| M001394240140300 | Length 30 cm | In distribution |
| M001394240120200 | Outer Diameter 12 mm | In distribution |
| M001394240180500 | Outer Diameter 18 mm | In distribution |
| M001394240030120 | Length 12 cm | In distribution |
| M001394240120300 | Length 30 cm | In distribution |
| M001394240100200 | Length 20 cm | In distribution |
| M001394240030060 | Outer Diameter 3 mm | In distribution |
| M001394240120500 | Length 50 cm | In distribution |
| M001394240060100 | Outer Diameter 6 mm | In distribution |
| M001394240140200 | Outer Diameter 14 mm | In distribution |
Same 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
| Clearance | Decision date |
|---|---|
| K261488 | 2026-07-24 |
| K253376 | 2025-10-30 |
| K242507 | 2024-10-03 |
| K230706 | 2023-06-27 |
| K213398 | 2022-04-12 |
| K141378 | 2014-10-08 |
| K133208 | 2013-11-14 |
| K132578 | 2013-09-13 |
| K113651 | 2012-01-11 |
| K112103 | 2011-08-12 |
| K102912 | 2011-03-03 |
| K110295 | 2011-03-03 |
| K102714 | 2011-02-11 |
| K060078 | 2006-01-31 |
| K040342 | 2004-04-13 |
| K034068 | 2004-03-26 |
Recalls
1 of these is Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|
| 2024-02-20 | Class I | Under Investigation by firm | An investigation determined that delivery of the Obsidio embolic using the aliquot technique for lower gastrointestinal bleeding embolization poses a high risk of bowel ischemia. The most serious and the most common adverse health consequen | 985 units |
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.
| 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.