Data / Medical devices / China / Beijing Konted Medical Technology Co., Ltd
Beijing Konted Medical Technology Co., Ltd: FDA-registered device maker in Beijing, China, 3 510(k) clearances
Beijing Konted Medical Technology Co., Ltd is registered with the FDA (registration 3027501622) in Beijing, China. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated July 23, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3027501622
- Address
- Room 111,1F, No. 27, Yong wang Road, Daxing Biological Building 3, Pharmaceutical Industry Base, Daxing District, Beijing, China, 102629
- Owner or operator
- Beijing Konted Medical Technology Co., Ltd (10089936)
- Roles
- Manufacturer
- First device listed
- January 24, 2024
- Registered through
- 2026
- Brand names listed
- Pocket Ultrasound System (Model: C10, C10HL, C10XL, C10XLpro, C10RC, C10HQ, C10CW, C10UC), Pocket Ultrasound System(Model: C10, C10TX, C10RL, C10RLpro), Portable Vein Finder, Ultrasound System, Wireless Ultrasound
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Vein Location, Liquid Crystal | KZA | 1 | Manufacturer | accessdata.fda.gov |
| System, Imaging, Pulsed Doppler, Ultrasonic | IYN | 2 | Manufacturer | accessdata.fda.gov |
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | 2 | Manufacturer | accessdata.fda.gov |
| Transducer, Ultrasonic, Diagnostic | ITX | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 23, 2026 | K261081 | Pocket Ultrasound System (C10MTpro,C10MXpro,C10MSpro,C10MBpro,C10MRpro) | IYN | Substantially Equivalent | Beijing Konted Medical Technology Co.,Ltd | accessdata.fda.gov |
| August 22, 2024 | K241979 | Pocket Ultrasound System (C10, C10TX, C10RL, C10RLpro) | IYN | Substantially Equivalent | Beijing Konted Medical Technology Co.,Ltd | accessdata.fda.gov |
| December 20, 2023 | K231354 | Pocket Ultrasound System (C10) | IYN | Substantially Equivalent | Beijing Konted Medical Technology Co.,Ltd | accessdata.fda.gov |
Compare with other makers
- All makers of System, Imaging, Pulsed Doppler, Ultrasonic
- All makers of Transducer, Ultrasonic, Diagnostic
- All makers of System, Imaging, Pulsed Echo, Ultrasonic
- All makers of Device, Vein Location, Liquid Crystal
Updated July 23, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.