F88

The F88 URE-SD/RD Flexible Ureteroscope is a handheld flexible ureteroscope offered in standard-deflection and reverse-deflection models. The FDA filing groups the two models under this…

Registry build 21.09.26

The F88 URE-SD/RD Flexible Ureteroscope is a handheld flexible ureteroscope offered in standard-deflection and reverse-deflection models. The FDA filing groups the two models under this device name and describes them as functionally identical except for tip-deflection direction.

The filing indicates the ureteroscope for endoscopic examination in the urinary tract, including examination of the kidney interior. It states that additional accessories can be used to perform diagnostic and therapeutic procedures.

Listed Item

Flexible Ureteroscope, Standard Deflection

Device Function and Design

The filing says the standard- and reverse-deflection models are functionally identical except for the direction of distal-tip deflection. It identifies the ureteroscope as reusable.

21manufacturers in China registered for this device type
6catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (10), Jiangsu (3), Shanghai (3). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FGB
Manufacturer City Province Registered as Device types
Guangdong MacroLux Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 9
Ningbo Wise Optomech Technology Corporation Ningbo Zhejiang Contract manufacturer 4
Shenzhen Hugemed Medical Technical Development Co., Ltd. Shenzhen Guangdong Manufacturer 22
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Suzhou Virgil Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Scivita Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 19
Macrolux Medical Technology Co., Ltd. Shenzhen Guangdong Manufacturer 9
Guangzhou RED Pine Medical Instrument Co., Ltd. Guangzhou Guangdong Manufacturer 8
Surgnova Healthcare Technologies (Zhejiang) Co., Ltd. Cixi Zhejiang Manufacturer 8
Zhuhai Pusen Medical Technology Co., Ltd. Zhuhai Guangdong Manufacturer 7
Shanghai Seegen Photoelectric Technology Co., Ltd. Shanghai Shanghai Manufacturer 7
Hunan Endoso Life Technology Co., Ltd. Xiangtan Hunan Manufacturer 7

Showing 12 of 21. All 21 manufacturers in China registered for Ureteroscope And Accessories, Flexible/Rigid

Record

Regulatory record for F88
Listed by SG Endoscopy PTE Ltd, Singapore
FDA product code FGB
Device type Ureteroscope And Accessories, Flexible/Rigid
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Repacker / relabeller, Manufacturer, Exporter
510(k) K243894
Record published 2025-06-30
Record revised 2025-07-21 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Hydrogen Peroxide
Prescription Prescription only
Label carries lot or batch number, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for F88
Catalogue number Size Per pack Status
0502388100 In distribution
0503388008 In distribution
0503388007 In distribution
0228388000 In distribution
0502388110 In distribution
0503388001 2 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Ureteroscope And Accessories, Flexible/Rigid Karl Storz GmbH & Co. KG 36
SemiFlex Scope Maxiflex, LLC 33
E-Line Richard Wolf Gmbh 28
Olympus Olympus Winter & IBE Gmbh 28
Uscope Zhuhai Pusen Medical Technology Co., Ltd. 23
WiScope® OTU Medical Inc 16
Redpine Guangzhou RED Pine Medical Instrument Co., Ltd. 16
LithoVue Boston Scientific Corporation 15
Single-use Flexible Ureteroscope Hunan Vathin Medical Instrument Co., Ltd. 14
Dornier MedTech Dornier Medtech America, Inc. 12
Innovex Shanghai AnQing Medical Instrument Co., Ltd. 12
Single Use Video Ureteroscope Direct In-Scope Suction Zhuhai Pusen Medical Technology Co., Ltd. 12

Showing 12 of 75. All products under Ureteroscope And Accessories, Flexible/Rigid

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K243894 2025-05-02

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