Flex

Rectoscope, Body Short

Registry build 21.09.26
9manufacturers in China registered for this device type
10catalogue numbers in this listing
2510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Shanghai (3), Guangdong (3), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code FDF
Manufacturer City Province Registered as Device types
Dalian Create Medical Products Co., Ltd. Dalian Liaoning Contract manufacturer 2
Yangzhou Fartley Medical Instrument Technology Co., Ltd. Yangzhou Jiangsu Contract manufacturer 24
Alton Shanghai Medical Instruments Co Ltd Shanghai Shanghai Complaint-file establishment 20
Hangzhou AGS MedTech Co., Ltd. Hangzhou Zhejiang Repacker / relabeller 19
BQ Plus Medical Co., Ltd. Songjiang Shanghai Contract manufacturer 13
Guangzhou RED Pine Medical Instrument Co., Ltd. Guangzhou Guangdong Manufacturer 8
Sonoscape Medical Corp. Shenzhen Guangdong Manufacturer 7
Shanghai Seegen Photoelectric Technology Co., Ltd. Shanghai Shanghai Manufacturer 7
Daichuan Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Manufacturer 2

Record

Regulatory record for Flex
Listed by Medrobotics Corporation, United States
FDA product code FDF
Device type Colonoscope And Accessories, Flexible/Rigid
Device class Class 2
Regulation 21 CFR 876.1500
Record published 2019-07-01
Record revised 2026-03-19 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, serial number

Catalogue Numbers

Catalogue numbers for Flex
Catalogue number Size Status
25171 In distribution
25171 In distribution
25171 In distribution
25171 In distribution
26470 In distribution
26471 In distribution
26472 In distribution
26114 In distribution
25171 In distribution
26473 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Fuse Endochoice, Inc. 52
Colonoscope And Accessories, Flexible/Rigid Karl Storz GmbH & Co. KG 51
Fujifilm Fujifilm Corporation 40
Pentax Hoya Corporation 37
Video Colonoscope Pentax of America, Inc. 25
G-EYE Colonoscope Smart Medical Systems Ltd. 24
Medisono Medisono, LLC 18
Evis Exera lll Colonovideoscope Olympus Medical Systems Corp. 16
Endoch Endoch Inc 14
Evis Exera II Colonovideoscope Olympus Medical Systems Corp. 12
Colonovideoscope Olympus Medical Systems Corp. 12
Colonoscope And Accessories, Flexible/Rigid Hangzhou AGS MedTech Co., Ltd. 10

Showing 12 of 115. All products under Colonoscope And Accessories, Flexible/Rigid

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K172036 2017-08-03
K162330 2017-05-04

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2019-01-25 Class II Process control The weld may break, resulting in the rod separating from the cone of the long and short cone Obturators. 24 2020-12-11
2019-01-25 Class II Process control The weld may break, resulting in the rod separating from the cone of the long and short cone Obturators. 35 2020-12-11

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