VersaCut+ Tissue Morcellator With Inverted Handpiece

The VersaCut+ Tissue Morcellator with Inverted Handpiece cuts and removes dissected tissue under direct or endoscopic visualization. It is intended for pelvic, laparoscopic, percutaneous…

Registry build 21.09.26

The VersaCut+ Tissue Morcellator with Inverted Handpiece cuts and removes dissected tissue under direct or endoscopic visualization. It is intended for pelvic, laparoscopic, percutaneous and open surgical procedures where access to the surgical site is limited.

A motor in the handpiece drives the cutting blades, while the control unit’s aspiration pump removes tissue through connected tubing. For endoscopic access, the device passes through a nephroscope sheath, with an adapter used as needed to keep the blades in view.

Preparation and Reuse

The system is supplied nonsterile. Before use, the handpiece, blade set and endoscope adapters require cleaning and sterilization. These components are designed for steam sterilization, with limited reuse of the handpieces and blade sets.

46manufacturers in China registered for this device type
1catalogue number
3510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Guangdong (15), Jiangsu (13), Zhejiang (7). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GCJ
Manufacturer City Province Registered as Device types
Hangzhou Kangji Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Hangzhou Endo Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 19
Beilun Plastech Inc Ningbo Zhejiang Contract manufacturer 13
Dongguan Honfield Precision Parts Co., Ltd. Zhangmutou, Dongguan Guangdong Contract manufacturer 8
Qingdao O-MEC Medical Technology Co., Ltd. Qingdao Shandong Contract manufacturer 6
Shenzhen Jingxintai Houseware Co., Ltd. Shenzhen Guangdong Contract manufacturer 6
MediConcepts Technology (Shenzhen) Company Limited Shenzhen Guangdong Contract manufacturer 5
Qisda Electronics (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Barco (Suzhou) Healthcare Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 4
Jiangsu Bana Medical Technology Co., Ltd. Changzhou Jiangsu Contract manufacturer 4
Comhuge Medical Wire AND Harness Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 2

Showing 12 of 46. All 46 manufacturers in China registered for Laparoscope, General & Plastic Surgery

Record

Regulatory record for VersaCut+ Tissue Morcellator with Inverted Handpiece
Listed by Lumenis, Ltd., Israel
FDA product code GCJ
Device type Laparoscope, General & Plastic Surgery
Device class Class 2
Regulation 21 CFR 876.1500
Establishment Specification developer, Manufacturer
510(k) K133272
Record published 2016-08-23
Record revised 2025-02-26 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for VersaCut+ Tissue Morcellator with Inverted Handpiece
Catalogue number Size Status
VersaCut+ Tissue Morcellator with Inverted Handpiece In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Elmed Elmed, Inc. 3,796
Surgical Direct Surgical Direct, Inc. 2,319
Novo Surgical Novo Surgical, Inc. 1,320
Elmed Incorporated Elmed, Inc. 911
Laparoscope, General & Plastic Surgery Karl Storz GmbH & Co. KG 774
Snowden-Pencer Steris Corporation 693
Millennium Avalign Technologies, Inc. 683
Hermann Medizintechnik GmbH Hermann Medizintechnik Gmbh 615
Clickline Karl Storz GmbH & Co. KG 582
V. Mueller Carefusion 2200, Inc. 553
Grasping forceps Sopro-Comeg GmbH 462
Gimmi Gimmi Gmbh 387

Showing 12 of 1,584. All products under Laparoscope, General & Plastic Surgery

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K133272 2014-05-13
K050639 2005-03-31
K980079 1998-04-09

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 VersaCut+ Tissue Morcellator with Inverted Handpiece
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Lumenis, Ltd. 510(k) number 2015-07-30 Class II Device Design There is a probability the hand piece may operate inconsistently and unpredictably during the morcellation procedure resulting in damage to non-target tissue. 54 devices with 108 hand pieces 2018-05-25

Recalls

1 of these is Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. 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
2013-01-02 Class I Labeling design Lumenis Ltd is recalling certain models of VersaCut Morcellator devices to perform corrective labeling as a result of three reported events of air embolism secondary to incorrect reversal tubing system hook-up. 931 units 2013-05-20

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