Ankor Endobronchial Tube

The ANKOR endobronchial tube is a double-lumen tube for differential ventilation. The FDA summary lists ABC35L among its named models. The filing says the tube is used for endobronchial…

Registry build 21.09.26

The ANKOR endobronchial tube is a double-lumen tube for differential ventilation. The FDA summary lists ABC35L among its named models.

The filing says the tube is used for endobronchial intubation and allows selective inflation or deflation of either lung.

Role and Configuration

The ANKOR design has two cuff configurations: ABC models include an additional ANKOR cuff, while HBC models do not.

The stated uses include thoracic surgery, bronchospirometry, and endobronchial anesthesia, as well as other uses requiring endobronchial intubation.

4manufacturers in China registered for this device type
8catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (2), Henan (1), Zhejiang (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code CBI
Manufacturer City Province Registered as Device types
Well Lead Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 46
Shenzhen Insighters Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
Henan Tuoren Medical Device Co., Ltd. Changyuan Henan Manufacturer 5
Hangzhou Tappa Medical Technology Co., Ltd. Hangzhou Zhejiang Manufacturer 3

Record

Regulatory record for Ankor endobronchial tube
Listed by Insung Medical Co., Ltd., South Korea
FDA product code CBI
Device type Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)
Device class Class 2
Regulation 21 CFR 868.5740
Establishment Manufacturer
510(k) K200968
Record published 2025-04-29

Specifications

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

Catalogue Numbers

Catalogue numbers for Ankor endobronchial tube
Catalogue number Size Status
ABC35L In distribution
ABC33L In distribution
ABC35R In distribution
ABC37L In distribution
ABC37R In distribution
ABC39R In distribution
ABC39L In distribution
ABC33R In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Insighters Shenzhen Insighters Medical Technology Co., Ltd. 39
Rusch Teleflex Medical LLC 26
Univent Tube (TCB Type) Fuji Systems Corp. 22
Hudson RCI Teleflex Medical LLC 21
Sheridan Teleflex Medical LLC 19
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector) Henan Tuoren Medical Device Co., Ltd. 18
Parker Flex-Tip Salter Labs 18
Parker Salter Labs 17
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector) Hangzhou Tappa Medical Technology Co., Ltd. 12
Forsure Forsure Medical Products LLC. 12
Endobronchial Tube Well Lead Medical Co., Ltd. 12
Portex ICU Medical, Inc 11

Showing 12 of 29. All products under Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K200968 2020-12-28

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