SonoScape

P60 Exp Series Digital Color Doppler Ultrasound System

Registry build 21.09.26
22manufacturers in China registered for this device type
111catalogue numbers in this listing
40510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (10), Jiangsu (5), Shandong (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code IYN
Manufacturer City Province Registered as Device types
Xuzhou Yongkang Electronic Science Technology Co., Ltd. Xuzhou Jiangsu Contract manufacturer 13
Xian Friendship Medical Electronics Co., Ltd. Xi’An Shaanxi 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
Contec Medical Systems Co., Ltd. Qinhuangdao Hebei Manufacturer 22
Shenzhen Viatom Technology Co., Ltd. Shenzhen Guangdong Manufacturer 9
Shantou Institute OF Ultrasonic Instruments Co., Ltd. Shantou Guangdong Contract manufacturer 8
Sonoscape Medical Corp. Shenzhen Guangdong Manufacturer 7
Carbon (Shenzhen) Medical Device Co., Ltd. Shenzhen Guangdong Manufacturer 6
Chison Medical Technologies Co., Ltd. Wuxi Jiangsu Contract manufacturer 5

Showing 12 of 22. All 22 manufacturers in China registered for System, Imaging, Pulsed Doppler, Ultrasonic

Record

Regulatory record for SonoScape
Listed by Sonoscape Medical Corp., China
FDA product code IYN
Device type System, Imaging, Pulsed Doppler, Ultrasonic
Device class Class 2
Regulation 21 CFR 892.1550
Establishment Manufacturer
510(k) K170999
Record published 2018-08-28
Record revised 2018-07-06 (version 4)

Specifications

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

Catalogue Numbers

Catalogue numbers for SonoScape
Catalogue number Size Status
EC9-5 In distribution
10I2 In distribution
6V3A In distribution
CWD8.0 In distribution
9L-A In distribution
VC2-9A In distribution
S20 In distribution
P9 In distribution
6CT-A In distribution
S2 In distribution
9L-A In distribution
VC2-9 In distribution
VE3-10 In distribution
L2-9 In distribution
P11 In distribution
CWD2.0 In distribution
BCC9-5 In distribution
6V1 In distribution
X11R In distribution
S8 In distribution
MPTEE In distribution
X11 In distribution
6CT-A In distribution
ML3-18 In distribution
C2-9 In distribution
X11U In distribution
MPTEE In distribution
12L-B In distribution
2P1 In distribution
C3-10V In distribution
L746 In distribution
P60 CV In distribution
P10 In distribution
X11 Plus In distribution
BCL10-5 In distribution
C1-6A In distribution
X11 Exp In distribution
PWD2.0 In distribution
P10 Plus In distribution
P22 In distribution
P60 Exp In distribution
X6 Pro In distribution
2P1 In distribution
VC6-2 In distribution
C361 In distribution
VC6-2 In distribution
6CT-A In distribution
6V3 In distribution
X6 In distribution
X11 Super In distribution
X11 Pro In distribution
P30 Pro In distribution
MPTEE mini In distribution
X11i In distribution
C322 In distribution
6V3A In distribution
LAP7 In distribution
P37 In distribution
12LT-A In distribution
LAP7 In distribution
BCC9-5 In distribution
MPTEE In distribution
X1 Pro In distribution
P40 Exp In distribution
L742 In distribution
7P-B In distribution
L746 In distribution
P40 In distribution
PWD2.0 In distribution
C351 In distribution
12LI-A In distribution
P50 S In distribution
12L-B In distribution
10L-I In distribution
18L-A In distribution
12LI-A In distribution
VC6-2 In distribution
P20 Pro In distribution
6CI-A In distribution
CWD2.0 In distribution
CWD5.0 In distribution
X3 In distribution
X11 Senior In distribution
18L-A In distribution
S6 In distribution
X5 Exp In distribution
10L-I In distribution
C613 In distribution
12C-ER In distribution
VL12-5 In distribution
13L-A In distribution
X11T In distribution
10I2 In distribution
C1-6 In distribution
8P1 In distribution
VE9-5 In distribution
S59 In distribution
3P-A In distribution
P50 Pro In distribution
13L-A In distribution
13L-A In distribution
6V7 In distribution
S60 Exp In distribution
L752 In distribution
C361 In distribution
3P-A In distribution
X11 Elite In distribution
6V7 In distribution
P30 S In distribution
X3 Pro In distribution
S60 VO In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Hisense Qingdao Hisense Medical Co., Ltd. 219
Medisono Medisono, LLC 173
Hisense Qingdao Hisense Medical Equipment Co., Ltd. 92
Diagnostic Ultrasound System Shenzhen Mindray BIO-Medical Electronics Co., Ltd. 89
Medistim Interconnect Cable Medistim ASA 40
Compact Cart Philips Ultrasound LLC 30
Siui Shantou Institute OF Ultrasonic Instruments Co., Ltd. 27
Clarius Ultrasound Scanner Clarius Mobile Health Corp. 25
Logiq GE Ultrasound Korea, Ltd. 25
Wisonic Shenzhen Wisonic Medical Technology Co., Ltd. 22
Vivid GE Vingmed Ultrasound A/S 21
HM70 EVO Samsung Medison Co., Ltd. 21

Showing 12 of 934. All products under System, Imaging, Pulsed Doppler, Ultrasonic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K254027 2026-08-24
K254028 2026-05-15
K252498 2025-12-05
K241949 2025-01-17
K222596 2023-02-10
K221089 2022-09-15
K221140 2022-09-13
K201059 2020-07-30
K182648 2019-01-29
K172993 2017-12-05
K173058 2017-12-01
K172082 2017-09-21
K170999 2017-07-12
K171000 2017-07-11
K170303 2017-05-19
K163427 2017-01-03
K160283 2016-04-04
K160258 2016-04-01
K152854 2016-01-13
K152396 2015-09-03
K152164 2015-08-28
K152165 2015-08-26
K150045 2015-04-28
K142714 2015-01-29
K142815 2015-01-28
K142710 2015-01-05
K142474 2014-12-19
K132527 2013-11-14
K132768 2013-10-04
K131213 2013-06-21
K130801 2013-06-14
K131088 2013-05-24
K130119 2013-04-12
K112602 2011-11-07
K112451 2011-09-16
K110510 2011-05-16
K102642 2011-03-04
K092922 2010-03-12
K052042 2005-08-09
K042369 2004-10-20

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P940005 1996-04-11 ULTRAMARK 9 HIGH DEFINITION IMAGING UULTRASOUND SYSTEM Advanced Technology Laboratories, Inc.

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