Data / Medical devices / United States / Magicare Tech Corp
Magicare Tech Corp: FDA-registered device maker in Ontario, CA, United States, 2 510(k) clearances
Magicare Tech Corp is registered with the FDA (registration 3016759113) in Ontario, CA, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated August 11, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016759113
- Address
- 1940 E Locust St Ste A, Ontario, CA, United States, 91761
- Owner or operator
- Cecilia Tech Inc (10068646)
- Roles
- Manufacturer
- First device listed
- March 9, 2022
- Registered through
- 2026
- Brand names listed
- MagiCare, MagiCare Face Shield (Made in USA), MagiCare Powder Free Blue Nitrile Examination Gloves
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mask, Surgical | FXX | 2 | Manufacturer | accessdata.fda.gov |
| Polymer Patient Examination Glove | LZA | 1 | Manufacturer | accessdata.fda.gov |
| Shield, Protective, Personnel | KPY | 1 | 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 |
|---|---|---|---|---|---|---|
| August 11, 2021 | K203152 | Disposable Face Mask | FXX | Substantially Equivalent | Chaozhou Cecilia Technology Co., Ltd. | accessdata.fda.gov |
| April 21, 2021 | K210145 | Nitrile Glove Powder Free Blue | LZA | Substantially Equivalent | Changzhou Universal Medical Equipment Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Mask, Surgical
- All makers of Shield, Protective, Personnel
- All makers of Polymer Patient Examination Glove
Updated August 11, 2021. 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.