Gynecare Versapoint

Resectoscopic System, Bridge - Hysteroscopic (Obturator - Visual)

Registry build 21.09.26
13manufacturers in China registered for this device type
16catalogue numbers in this listing
1510(k) clearance
1recall

Who Else Makes It

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

Chinese manufacturers registered for FDA product code HIH
Manufacturer City Province Registered as Device types
Guangdong MacroLux Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 9
Peter’s Technology (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 9
Qingdao O-MEC Medical Technology Co., Ltd. Qingdao Shandong Contract manufacturer 6
Ningbo Skonsin Electronics Ltd. Ningbo Zhejiang Contract manufacturer 1
Hangzhou Fushan Medical Appliance Co., Ltd. Hangzhou Zhejiang Contract manufacturer 44
Zhejiang Huanyi Sterilization Technology Co., Ltd. Huzhou Zhejiang Contract manufacturer 25
Macrolux Medical Technology Co., Ltd. Shenzhen Guangdong Manufacturer 9
Guangzhou RED Pine Medical Instrument Co., Ltd. Guangzhou Guangdong Manufacturer 8
Shanghai AnQing Medical Instrument Co., Ltd. Shanghai Shanghai Manufacturer 5
Guangdong EO Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 5
Suzhou Acuvu Medical Technology Co., Ltd. Suzhou Jiangsu Specification developer 4
Jiangsu Jiyuan Medical Technology Co., Ltd. Taizhou Jiangsu Specification developer 3

Showing 12 of 13. All 13 manufacturers in China registered for Hysteroscope (And Accessories)

Record

Regulatory record for Gynecare Versapoint
Listed by Ethicon, Inc., United States
FDA product code HIH
Device type Hysteroscope (And Accessories)
Device class Class 2
Regulation 21 CFR 884.1690
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
510(k) K962482
Record published 2016-09-16
Record revised 2025-07-17 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date, serial number
Storage Storage environment temperature up to 25 °C; Special storage condition: Keep dry; Special storage condition: Fragile, handle with care
Packaging Box of 5, carton of 20
Distribution end date 2021-12-24

Catalogue Numbers

Catalogue numbers for Gynecare Versapoint
Catalogue number Size Status
01938 Withdrawn
01735 Withdrawn
00464 Withdrawn
00465 Withdrawn
00463 Withdrawn
01950 Withdrawn
00467 Withdrawn
01934 Withdrawn
00468 Withdrawn
00480 Withdrawn
01985 Withdrawn
01931 Withdrawn
00466 Withdrawn
01936 Withdrawn
01939 Withdrawn
00481 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Hysteroscope (And Accessories) Karl Storz GmbH & Co. KG 255
AED National Advanced Endoscopy Devices, Inc. 79
USA Elite Gyrus Acmi, Inc. 79
Olympus Olympus Winter & IBE Gmbh 57
Hysteroscope (And Accessories) Stryker GmbH 42
TruClear Covidien LP 29
Hysteroscopy sheath Sopro-Comeg GmbH 28
Hysteroscope (And Accessories) Richard Wolf Gmbh 24
Hysteroscope Sopro-Comeg GmbH 18
Elite 2 System Gyrus Acmi, Inc. 17
USA Elite System Gyrus Acmi, Inc. 11
SlimLine Gyrus Acmi, Inc. 10

Showing 12 of 177. All products under Hysteroscope (And Accessories)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K994418 2000-01-24

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 Gynecare Versapoint
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Ethicon, Inc. 510(k) number 2004-12-16 Not classified Nonconforming Material/Component Deformation of the Verspoint Hysteroscopic System Connector Cable hand grips when autoclaved causing possible non-sterile electrodes. 891electrodes 2005-10-31

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