Data / Medical devices / China / Miconvey Technologies Co., Ltd.
Miconvey Technologies Co., Ltd.: FDA-registered device maker in Chongqing, China, 2 510(k) clearances
Miconvey Technologies Co., Ltd. is registered with the FDA (registration 3014932737) in Chongqing, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 30, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014932737
- Address
- No.16, Fangzheng Avenue, Beibei District, Chongqing, China, 400714
- Owner or operator
- Miconvey Technologies Co., Ltd. (10058356)
- Roles
- Manufacturer
- First device listed
- August 30, 2018
- Registered through
- 2026
- Brand names listed
- Miconvey Technologies Co., Ltd., Ultrasonic Surgical System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Instrument, Ultrasonic Surgical | LFL | U | Manufacturer | accessdata.fda.gov |
| Staple, Implantable | GDW | 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 |
|---|---|---|---|---|---|---|
| September 30, 2022 | K210567 | Ultrasonic Surgical System | LFL | Substantially Equivalent | Miconvey Technologies Co., Ltd. | accessdata.fda.gov |
| March 3, 2017 | K162947 | Disposable End-to-end Anastomosis Circular Stapler; Universal Endoscopic Linear Cutting Stapler and Single Use Loading Unit; Linear Cutting Stapler and Single Use Loading Unit; Disposal Hemorrhoidal Circular Stapler | GDW | Substantially Equivalent | Chongqing Qmi Surgical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated September 30, 2022. 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.