ClearView Uterine Manipulator

ClearView Uterine Manipulator, regular tip

Registry build 21.09.26
5manufacturers in China registered for this device type
4catalogue numbers in this listing
2510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Guangdong (2), Zhejiang (2), Beijing (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LKF
Manufacturer City Province Registered as Device types
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Tonglu Qianyan Medtech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Modern Medical Equipment Manufacturing (Qing Yuan) Ltd Qing Yuan Guangdong Contract manufacturer 26
Zhejiang Huanyi Sterilization Technology Co., Ltd. Huzhou Zhejiang Contract manufacturer 25
Beijing Hangtian Kadi Technology R&D Institute Beijing Beijing Manufacturer 5

Record

Regulatory record for ClearView Uterine Manipulator
Listed by Clinical Innovations, LLC, United States
FDA product code LKF
Device type Cannula, Manipulator/Injector, Uterine
Device class Class 2
Regulation 21 CFR 884.4530
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
510(k) K940681
Record published 2016-09-01
Record revised 2018-12-07 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Pack of 4, pack of 5

Catalogue Numbers

Catalogue numbers for ClearView Uterine Manipulator
Catalogue number Size Status
UM201 In distribution
UM700 In distribution
UM202 In distribution
UM900 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Elmed Elmed, Inc. 39
Cannula, Manipulator/Injector, Uterine C R I 31
Marina Medical Marina Medical Instruments, Inc. 29
HSG Catheter Titus Medical LLC 26
HNM Women Care HNM Stainless, LLC. 20
Bioteque Bioteque Taiwan Ltd. 16
Viky Endocontrol 15
Cannula, Manipulator/Injector, Uterine Panpac Medical Corporation 14
Uterine ElevatOR Pro THE O R Company PTY Ltd 12
Valtchev Uterine Mobilizer Conkin Surgical Instruments Ltd. 10
Novo Surgical Novo Surgical, Inc. 9
McCarus-Volker Fornisee® System LSI Solutions Inc. 9

Showing 12 of 111. All products under Cannula, Manipulator/Injector, Uterine

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K131781 2014-05-28
K940681 1994-07-26

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of ClearView Uterine Manipulator
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Clinical Innovations, LLC 510(k) number 2008-05-12 Not classified Process control Inadequate package seal could compromise sterility. 260 units 2008-09-25
Clinical Innovations, LLC 510(k) number 2008-05-12 Not classified Process control Inadequate package seal could compromise sterility. 500 units 2008-09-25

Recalls

1 of these is 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
2019-05-30 Class II Process control An incorrect component used during manufacturing. The uterine manipulator tip support does not have the “notch” required to attach the spacer and or colpotomy cup. This may result in a delay in surgery and additional surgical interventions 280 devices 2020-08-24

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