Flex Vessel Prep System

FLEX Vessel Prep System, FSC 4-120

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (2), Jiangsu (1).

Chinese manufacturers registered for FDA product code PNO
Manufacturer City Province Registered as Device types
OrbusNeich Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Complaint-file establishment 5
Brosmed Medical Co., Ltd. Dongguan Guangdong Contract manufacturer 4
DK Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 3

Record

Regulatory record for Flex Vessel Prep System
Listed by Venturemed Group, Inc, United States
FDA product code PNO
Device type Catheter, Percutaneous, Cutting/Scoring
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Specification developer, Complaint-file establishment, Manufacturer
Record published 2019-06-27
Record revised 2023-04-21 (version 3)

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
Sizes Catheter length 75 cm

Catalogue Numbers

Catalogue numbers for Flex Vessel Prep System
Catalogue number Size Status
FSC 4-120 In distribution
FSC 4-40 In distribution
FSC 4-75 Catheter Length 75 cm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Tri-Wedge PTA Scoring Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 168
PTA Scoring Balloon Dilatation Catheter DK Medical Technology Co., Ltd. 120
VascuTrak® Bard Peripheral Vascular, Inc. 109
Ultrascore Bard Peripheral Vascular, Inc. 103
Scoreflex PTA Scoring Balloon Catheter OrbusNeich Medical (Shenzhen) Co., Ltd. 58
AngioSculpt® Spectranetics Corp. 51
Aperta NSE™ PTA Balloon Dilatation Catheter Goodman Co., Ltd. 38
AngioSculpt OTW PTA Scoring Balloon Catheter The Spectranetics Corp. 25
Serranator Cagent Vascular 18
AngioSculpt OTW PTA Scoring Balloon Catheter with HydroCross Coating The Spectranetics Corp. 13
Advance Enforcer Cook Incorporated 12
2cm Peripheral Cutting Balloon® Boston Scientific Corporation 12

Showing 12 of 16. All products under Catheter, Percutaneous, Cutting/Scoring

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K202187 2020-09-11
K152789 2016-05-25

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