Data / Medical devices / China / Avantsonic Technology Co., Ltd.
Avantsonic Technology Co., Ltd.: FDA-registered device maker in Chongqing, China, 2 510(k) clearances
Avantsonic Technology Co., Ltd. is registered with the FDA (registration 3014432311) in Chongqing, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 29, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014432311
- Address
- 2F, Building 4A, No. 21, Changkang Road, Yuzui Town, Liangjiang New Area, Chongqing, China, 401133
- Owner or operator
- AvantSonic Technology Co., Ltd. (10058076)
- Roles
- Manufacturer
- First device listed
- July 4, 2018
- Registered through
- 2026
- Brand names listed
- Bladder Scanner(AS-1), Bladder Scanner(AS-2), Bladder Scanner(Model: Z3, Z5)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| 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 |
|---|---|---|---|---|---|---|
| December 29, 2023 | K230986 | Bladder Scanner | IYO | Substantially Equivalent | Avantsonic Technology Co., Ltd. | accessdata.fda.gov |
| January 24, 2018 | K171528 | Bladder Scanner (model: PadScan DS3, PadScan Z3, PadScan Z5) | IYO | Substantially Equivalent | Avantsonic Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Transducer, Ultrasonic, Diagnostic
- All makers of System, Imaging, Pulsed Echo, Ultrasonic
Updated December 29, 2023. 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.