NGB-006 Needle-Guided Bracket/PLAS/VET

Catalogue number 120-002155-00, listed by Shenzhen Mindray BIO-Medical Electronics Co., Ltd., China, under System, Imaging, Pulsed Doppler, Ultrasonic. 22 manufacturers in China are registered for this product code.

Registry build 21.09.26
22manufacturers in China registered for this device type
1catalogue number
83510(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 NGB-006 Needle-guided Bracket/PLAS/VET
Listed by Shenzhen Mindray BIO-Medical Electronics Co., Ltd., China
FDA product code IYN
Device type System, Imaging, Pulsed Doppler, Ultrasonic
Device class Class 2
Regulation 21 CFR 892.1550
Establishment Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k) K140030
Record published 2016-09-20
Record revised 2022-06-10 (version 6)

Specifications

Specifications
MRI safety MR Unsafe
Sterilisation Hydrogen Peroxide
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for NGB-006 Needle-guided Bracket/PLAS/VET
Catalogue number Size Status
120-002155-00 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
SonoScape Sonoscape Medical Corp. 111
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

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
K260846 2026-05-11
K253049 2026-02-11
K251601 2025-12-03
K251853 2025-11-07
K251820 2025-09-12
K251250 2025-09-05
K251192 2025-08-22
K250024 2025-05-30
K250020 2025-05-19
K250110 2025-05-16
K242231 2024-11-08
K241201 2024-09-16
K241432 2024-09-12
K240906 2024-07-23
K240684 2024-06-17
K240115 2024-04-22
K231685 2023-10-26
K230768 2023-06-09
K222928 2023-02-07
K221300 2022-09-29
K221496 2022-09-29
K220242 2022-03-25
K220051 2022-03-04
K212265 2021-11-16
K212900 2021-11-05
K211337 2021-07-01
K210699 2021-06-10
K210416 2021-06-10
K203391 2021-03-23
K201990 2020-11-09
K201693 2020-08-21
K200643 2020-07-24
K200979 2020-05-28
K200001 2020-04-09
K200411 2020-04-08
K200251 2020-04-02
K192410 2019-12-19
K192152 2019-12-13
K183660 2019-04-09
K183377 2019-04-04
K190206 2019-03-08
K182636 2019-01-10
K181637 2019-01-09
K182603 2018-11-14
K180912 2018-07-30
K173471 2018-01-08
K172860 2018-01-02
K172970 2017-10-25
K171579 2017-10-18
K171891 2017-09-21
K171034 2017-07-10
K163690 2017-04-20
K170277 2017-03-23
K162845 2016-12-15
K162267 2016-09-06
K161525 2016-07-13
K160381 2016-03-09
K152543 2015-10-29
K152763 2015-10-21
K152545 2015-10-02
K150080 2015-06-12
K150204 2015-04-10
K143472 2015-01-02
K141010 2014-05-14
K140030 2014-02-19
K132779 2013-11-19
K132341 2013-08-15
K130833 2013-06-21
K130695 2013-06-19
K123503 2012-12-13
K122010 2012-07-20
K121010 2012-04-19
K120699 2012-04-19
K113647 2011-12-16
K110199 2011-02-08
K103677 2011-01-31
K103583 2010-12-27
K100830 2010-05-05
K083505 2008-12-12
K083001 2008-10-22
K081320 2008-05-27
K080640 2008-03-21
K063500 2006-12-06

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