Data / Medical devices / China / Alliedstar Medical Equipment Co., Ltd.
Alliedstar Medical Equipment Co., Ltd.: FDA-registered device maker in Ziyang Sichuan, China, 1 510(k) clearance
Alliedstar Medical Equipment Co., Ltd. is registered with the FDA (registration 3018994222) in Ziyang Sichuan, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 14, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3018994222
- Address
- Floor 3-4, Unit 2, Building 3, No.222, West third section, Waihuan Road, Yanjiang District, Ziyang Sichuan, China, 641300
- Owner or operator
- Alliedstar Medical Equipment Co., Ltd. (10081371)
- Roles
- Manufacturer
- First device listed
- April 7, 2021
- Registered through
- 2027
- Brand names listed
- AS 100, AS 200E, AS 260, AS 260a, DI-1, DIP-3, DIP-A, DIP-D and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Sterilization Wrap Containers, Trays, Cassettes & Other Accessories | KCT | 2 | Manufacturer | accessdata.fda.gov |
| System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations | NOF | 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 |
|---|---|---|---|---|---|---|
| October 14, 2026 | K262042 | Sterilization Cassette (CASS-1) | KCT | Substantially Equivalent | Alliedstar Medical Equipment Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations
Updated October 14, 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.