Embotrap

EMBOTRAP III 6.5 x 45 mm Revascularization Device

Registry build 21.09.26
5manufacturers in China registered for this device type
5catalogue numbers in this listing
5510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shanghai (3), Jiangsu (2). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code NRY
Manufacturer City Province Registered as Device types
Covidien Medical Products (Shanghai) Manufacturing LLC Shanghai Shanghai Contract manufacturer 8
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Suzhou Zenith Vascular Scitech Limited Suzhou Jiangsu Manufacturer 6
Shanghai Wallaby Medical Technologies Co., Inc. Shanghai Shanghai Contract manufacturer 5

Record

Regulatory record for Embotrap
Listed by Neuravi Limited, Ireland
FDA product code NRY
Device type Catheter, Thrombus Retriever
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Specification developer, Manufacturer
510(k) K193063
Record published 2020-07-16
Record revised 2025-12-15 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for Embotrap
Catalogue number Size Status
ET309522 In distribution
ET309537 In distribution
ET009521 In distribution
ET309645 In distribution
ET009533 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Penumbra System Penumbra Inc. 100
RED 43 Penumbra Inc. 18
Solitaire™ X-Pack Micro Therapeutics, Inc. 14
ACE Penumbra Inc. 14
Raptor Aspiration Catheter Balt USA, LLC 13
Cereglide Cerenovus, Inc. 13
Solitaire™ Micro Therapeutics, Inc. 9
Solitaire™ X Micro Therapeutics, Inc. 9
RED 68 Penumbra Inc. 9
Riptide™ Micro Therapeutics, Inc. 9
Zoom™ Reperfusion Catheter Imperative Care Inc. 9
CaptureTM Micro Therapeutics, Inc. 8

Showing 12 of 80. All products under Catheter, Thrombus Retriever

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K251789 2025-09-25
K212908 2021-10-13
K211338 2021-07-30
K193063 2020-07-14
K173452 2018-05-09

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