2.0 Mm OTW B-Laser™ Catheter

2.0 mm OTW B-Laser™ catheter For Infra Inguinal Atherectomy

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
8510(k) clearances naming this product code

Who Else Makes It

All of them in Guangdong. 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MCW
Manufacturer City Province Registered as Device types
ATL Technology DG,Ltd. Dongguan Guangdong Contract manufacturer 14
Quasar Electronics Technology (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 2
Dongguan King Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 14

Record

Regulatory record for 2.0 mm OTW B-Laser™ catheter
Listed by Eximo Medical Ltd, Israel
FDA product code MCW
Device type Catheter, Peripheral, Atherectomy
Device class Class 2
Regulation 21 CFR 870.4875
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K181642
Record published 2019-03-22
Record revised 2024-11-05 (version 3)

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, serial number
Packaging Master carton box of 11
Distribution end date 2023-12-28

Catalogue Numbers

Catalogue numbers for 2.0 mm OTW B-Laser™ catheter
Catalogue number Size Status
EXM-4003-0000 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Diamondback Peripheral Cardiovascular Systems Incorporated 44
Turbo-Elite™ Spectranetics Corp. 24
Stealth Cardiovascular Systems Incorporated 20
Zilient Cardiovascular Systems Incorporated 16
TurboHawk Covidien LP 15
HawkOne Covidien LP 14
Turbo-Elite Laser Atherectomy Catheter Spectranetics Corp. 12
SilverHawk Covidien LP 11
Auryon Atherectomy Catheter Eximo Medical Ltd 10
Revolution Peripheral Atherectomy System Rex Medical 8
Peripheral RotaLink® Plus Boston Scientific Corporation 8
SilverHawkTM Covidien LP 8

Showing 12 of 102. All products under Catheter, Peripheral, Atherectomy

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K260244 2026-04-10
K241553 2024-06-27
K233668 2023-12-15
K230709 2023-06-09
K220116 2022-09-26
K221077 2022-06-09
K202835 2020-12-02
K181642 2018-10-05

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