Vis-Rx Prime

The Vis-Rx Prime Micro-Imaging Catheter obtains optical images inside coronary arteries as part of the Gentuity HF-OCT Imaging System. A rotating optical fiber and lens assembly delivers…

Registry build 21.09.26

The Vis-Rx Prime Micro-Imaging Catheter obtains optical images inside coronary arteries as part of the Gentuity HF-OCT Imaging System. A rotating optical fiber and lens assembly delivers near-infrared light to vessel tissue and receives the reflected light used to form images.

An external sheath houses the optical imaging core and supports catheter placement. The rapid-exchange catheter accepts a 0.014-inch guidewire and connects to the console’s Probe Interface Module. It is supplied sterile for single use with a 3 ml purge syringe.

Listed Item

1.8F Rapid exchange micro-imaging high-frequency OCT catheter kit – US

Imaging Scope

The catheter is intended for vessels 1.3 to 6.0 mm in diameter, before or after transluminal interventional procedures in appropriate candidates. It is not intended for a target vessel that has previously undergone bypass surgery.

11manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (5), Guangdong (3), Zhejiang (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DQO
Manufacturer City Province Registered as Device types
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Amsino Medical (Kunshan) Co., Ltd. Kunshan Jiangsu Contract manufacturer 53
Conod Medical Shuyang Co., Ltd. Shuyang Jiangsu Contract manufacturer 22
Bioxin Medical Co., Ltd. Weihai Shandong Contract manufacturer 8
GRI Medical & Electronic Technology Co., Ltd. Jiaxing Zhejiang Contract manufacturer 71
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Wuxi Goals Medical Technology Co., Ltd. Yixing Jiangsu Contract manufacturer 24
Sunny Medical Device (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Shenzhen Vivolight Medical Device&Technology Co., Ltd. Shenzhen Guangdong Manufacturer 4
Shenzhen Antmed Co., Ltd. Dongguan Guangdong Manufacturer 4

Record

Regulatory record for Vis-Rx Prime
Listed by Gentuity, LLC, United States
FDA product code DQO
Device type Catheter, Intravascular, Diagnostic
Device class Class 2
Regulation 21 CFR 870.1200
Establishment Complaint-file establishment, Manufacturer
510(k) K242966
Record published 2025-04-09

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date, manufacturing date
Sizes Catheter gauge 1.8 Fr

Catalogue Numbers

Catalogue numbers for Vis-Rx Prime
Catalogue number Size Status
G31 Catheter Gauge 1.8 Fr In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Performa® Merit Medical Systems, Inc. 1,101
Impress® Merit Medical Systems, Inc. 839
Super Torque Cordis Corp. 611
Soft-Vu AngioDynamics, Inc. 591
Torcon NB Cook Incorporated 463
Mariner AngioDynamics, Inc. 323
INT,SlideCath Shanghai Kindly Medical Instruments Co., Ltd. 264
Infiniti Cordis Corp. 251
Infiniti Cordis US Corp. 241
AngiOptic AngioDynamics, Inc. 227
Tempo Cordis Corp. 217
SiteSeer™ Medtronic, Inc. 204

Showing 12 of 226. All products under Catheter, Intravascular, Diagnostic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242966 2025-01-31
K230620 2023-08-08

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Vis-Rx Prime
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Gentuity, LLC 510(k) number 2026-03-23 Class II Device Design The potential for repeated frames during HF-OCT pullback when using the Gentuity HF-OCT Console (software version 21.11 to 23.3.13) with the Vis-Rx and Vis-Rx Prime catheters. This correction is intended to ensure that users are fully infor 184 units (28 US, 156 OUS)

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