Vivid

Vivid S70N S60N v204 to v205 Upg kit

Registry build 21.09.26
37manufacturers in China registered for this device type
16catalogue numbers in this listing

Who Else Makes It

Concentrated in Guangdong (14), Jiangsu (9), Shanghai (3). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code IYO
Manufacturer City Province Registered as Device types
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Raise Medical Industries, Inc. Foshan Guangdong Contract manufacturer 16
ATL Technology DG,Ltd. Dongguan Guangdong Contract manufacturer 14
Xuzhou Yongkang Electronic Science Technology Co., Ltd. Xuzhou Jiangsu Contract manufacturer 13
Taijia Medical Electronics (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
Philips Ultrasound (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 5
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Taizhou City K&W International Trade Co., Ltd. Jiangyan Jiangsu Repacker / relabeller 38
Contec Medical Systems Co., Ltd. Qinhuangdao Hebei Manufacturer 22
Sterigenics Shanghai E Beam Ltd. Shanghai Shanghai Contract manufacturer 14

Showing 12 of 37. All 37 manufacturers in China registered for System, Imaging, Pulsed Echo, Ultrasonic

Record

Regulatory record for Vivid
Listed by GE Vingmed Ultrasound A/S, Norway
FDA product code IYO
Device type System, Imaging, Pulsed Echo, Ultrasonic
Device class Class 2
Regulation 21 CFR 892.1560
Establishment Specification developer, Manufacturer
510(k) K150087
Record published 2016-08-01
Record revised 2026-04-29 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, manufacturing date, serial number
Storage Handling environment atmospheric pressure 70 to 106 KiloPascal; Handling environment humidity 30 to 95 % RH; Handling environment temperature 10 to 35 °C; Storage environment temperature -20 to 60 °C; Storage environment atmospheric pressure 70 to 106 KiloPascal
Distribution end date 2020-04-01

Catalogue Numbers

Catalogue numbers for Vivid
Catalogue number Size Status
E90 v201 In distribution
S70N v206 In distribution
E80 v202 In distribution
E90 v203 with LCD In distribution
S60N v206CH In distribution
E90 v204 with OLED In distribution
S60N v205 In distribution
E v202 to v203 UPG In distribution
E v204 4D ICE UPG In distribution
E80 v203 with OLED In distribution
S70N v206CH In distribution
S v204 to v205 UPG In distribution
S70N v202CH In distribution
S60N v202CH In distribution
S70N v204 In distribution
E9 BT11 and BT12 to BT13 XDclear UPG Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Hitachi Hitachi, Ltd. 224
eTRAX™ Needle Civco Medical Instruments Co., Inc. 43
BladderScan® Verathon Inc. 38
Verza Guidance System Civco Medical Instruments Co., Inc. 37
Needle Guide Civco Medical Instruments Co., Inc. 34
Siui Shantou Institute OF Ultrasonic Instruments Co., Ltd. 34
Biopsy Bracket Civco Medical Instruments Co., Inc. 33
Tracking Bracket Starter Kit Civco Medical Instruments Co., Inc. 29
System, Imaging, Pulsed Echo, Ultrasonic GE Healthcare Japan Corporation 23
eTRAX™ Needle System Starter Kit Civco Medical Instruments Co., Inc. 20
Tracking Bracket Civco Medical Instruments Co., Inc. 19
Logiq GE Ultrasound Korea, Ltd. 18

Showing 12 of 805. All products under System, Imaging, Pulsed Echo, Ultrasonic

Recalls Naming This Product

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

Recalls naming the identifiers of Vivid
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
GE Vingmed Ultrasound A/S 510(k) number 2024-05-02 Class II Device Design GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed on the ultrasound scanner screen rather than the in 7 units
GE Vingmed Ultrasound A/S 510(k) number 2023-05-30 Class II Process design GE HealthCare has become aware that certain Vivid ultrasound systems cannot boot up in a timely fashion. If this occurs, it can delay availability of the device in time-critical emergency situations.
GE Vingmed Ultrasound A/S 510(k) number 2023-05-30 Class II Process design GE HealthCare has become aware that certain Vivid ultrasound systems cannot boot up in a timely fashion. If this occurs, it can delay availability of the device in time-critical emergency situations.
GE Medical Systems Ultrasound and Primary Care Diagnostics LLC 510(k) number 2018-03-22 Class II Component design/selection The system side of the power cord may break and expose the electrical conductors leading to the risk of shock. 12,426 (4,717 US; 7,709 OUS ALL PRODUCTS) 2021-08-24
GE Medical Systems Ultrasound and Primary Care Diagnostics LLC 510(k) number 2018-03-22 Class II Component design/selection The system side of the power cord may break and expose the electrical conductors leading to the risk of shock. 12,426 (4,717 US; 7,709 OUS ALL PRODUCTS) 2021-08-24
GE Medical Systems Ultrasound and Primary Care Diagnostics LLC 510(k) number 2018-03-22 Class II Component design/selection The system side of the power cord may break and expose the electrical conductors leading to the risk of shock. 12,426 (4,717 US; 7,709 OUS ALL PRODUCTS) 2021-08-24
GE Medical Systems, LLC 510(k) number 2017-03-10 Class II Software design GE Healthcare has become aware of an issue where a patient other than the intended is incorrectly selected by the operator in situations where DICOM Worklist search response time is slow. This issue is limited to certain Vivid Ultrasound sy 971(412 US; 559 OUS) 2018-03-12
GE Medical Systems, LLC 510(k) number 2017-03-10 Class II Software design GE Healthcare has become aware of an issue where a patient other than the intended is incorrectly selected by the operator in situations where DICOM Worklist search response time is slow. This issue is limited to certain Vivid Ultrasound sy 396 (67 US; 329 OUS) 2018-03-12

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