Ichor

The ICHOR embolectomy system is indicated for the non-surgical removal of emboli and thrombi from blood vessels. The device is intended for the peripheral vasculature.

Registry build 21.09.26
1manufacturer
2catalogue numbers in this listing

Who Else Makes It

Registered in Shandong.

Chinese manufacturers registered for FDA product code DXE
Manufacturer City Province Registered as Device types
Bioxin Medical Co., Ltd. Weihai Shandong Contract manufacturer 8

Record

Regulatory record for Ichor
Listed by Ichor Vascular Inc, United States
FDA product code DXE
Device type Catheter, Embolectomy
Device class Class 2
Regulation 21 CFR 870.5150
Establishment Specification developer, Manufacturer
510(k) K230743
Record published 2023-10-13
Record revised 2023-05-19 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment temperature 70 to 75 °F
Distribution end date 2023-05-18

Catalogue Numbers

Catalogue numbers for Ichor
Catalogue number Size Status
ICH14FR Catheter Gauge 14F Fr In distribution
ICH7FR Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
LeMaitre Embolectomy Catheter Lemaitre Vascular, Inc. 68
LMI Arterial Embolectomy Catheter Lucas Medical, Inc. 63
Indigo System Penumbra Inc. 60
Fogarty Edwards Lifesciences Technology Sarl 44
Arrow Teleflex Medical LLC 28
Bard Latex-free Arterial Embolectomy Catheters Applied Medical Resources Corp. 22
Biosensors Embolectomy Catheter Bioptimal International Pte. Ltd. 16
Amplatz Goose Neck Covidien LP 15
Amplatz Goose Neck™ ev3, Inc. 13
LMI Thrombectomy Catheter Lucas Medical, Inc. 12
LMI Occlusion Catheter Lucas Medical, Inc. 12
Syntel Thrombectomy Catheter Applied Medical Resources Corp. 9

Showing 12 of 88. All products under Catheter, Embolectomy

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