Ruby Coil

Ruby Extra Soft, 2x10

Registry build 21.09.26
6manufacturers in China registered for this device type
66catalogue numbers in this listing
1510(k) clearance

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 Ruby Coil
Listed by Penumbra Inc., United States
FDA product code KRD
Device type Device, Vascular, For Promoting Embolization
Device class Class 2
Regulation 21 CFR 870.3300
Establishment Manufacturer, Exporter
510(k) K173614
Record published 2018-05-15
Record revised 2026-07-14 (version 3)

Specifications

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

Catalogue Numbers

Catalogue numbers for Ruby Coil
Catalogue number Size Status
RBY6C0406-B In distribution
RBY2C0415-B In distribution
RBY6C0204-B In distribution
RBY2C1440-B In distribution
RBY6C0202-B In distribution
RBY4C1035-B In distribution
RBY2C0740-B In distribution
RBY6C0210-B In distribution
RBY4C0202-B In distribution
RBY2C0410-B In distribution
RBY2C0840-B In distribution
RBY2C0420-B In distribution
RBY2C3660-B In distribution
RBY4C0620-B In distribution
RBY2C3260-B In distribution
RBY2C0430-B In distribution
RBY2C0930-B In distribution
RBY4C0208-B In distribution
RBY2C0630-B In distribution
RBY2C1035-B In distribution
RBY2C1240-B In distribution
RBY4C0305-B In distribution
RBY2C0512-B In distribution
RBY4C0660-B In distribution
RBY2C0305-B In distribution
RBY4C0201-B In distribution
RBY6C0415-B In distribution
RBY2C2457-B In distribution
RBY2C0535-B In distribution
RBY4C0860-B In distribution
RBY2C0825-B In distribution
RBY6C0315-B In distribution
RBY2C1060-B In distribution
RBY2C1660-B In distribution
RBY4C0415-B In distribution
RBY6C0201-B In distribution
RBY2C1460-B In distribution
RBY2C0612-B In distribution
RBY2C0530-B In distribution
RBY2C0312-B In distribution
RBY4C2060-B In distribution
RBY2C0725-B In distribution
RBY4C0315-B In distribution
RBY4C0835-B In distribution
RBY2C1260-B In distribution
RBY6C0620-B In distribution
RBY2C1857-B In distribution
RBY6C0208-B In distribution
RBY2C0520-B In distribution
RBY4C0212-B In distribution
RBY2C0640-B In distribution
RBY2C0435-B In distribution
RBY4C0204-B In distribution
RBY4C0406-B In distribution
RBY2C0320-B In distribution
RBY2C0620-B In distribution
RBY4C0630-B In distribution
RBY2C2860-B In distribution
RBY4C1650-B In distribution
RBY4C1260-B In distribution
RBY6C0305-B In distribution
RBY4C0210-B In distribution
RBY4C1240-B In distribution
RBY6C0630-B In distribution
RBY6C0212-B In distribution
RBY2C4060-B 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
K250079 2025-03-14

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