Data / Medical devices / United States / Sota Cloud Corporation
Sota Cloud Corporation: FDA-registered device maker in Orange, CA, United States, 2 510(k) clearances
Sota Cloud Corporation is registered with the FDA (registration 3034604691) in Orange, CA, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 3, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3034604691
- Address
- 1073 N Batavia St Ste B, Orange, CA, United States, 92867
- Owner or operator
- SOTA Cloud Corporation (10092262)
- Roles
- Manufacturer
- First device listed
- December 18, 2024
- Registered through
- 2027
- Brand names listed
- SOTA Cloud, SOTA Cloud Smart Camera, SOTA Cloud Smart Sensor
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 2 | Manufacturer | accessdata.fda.gov |
| System, X-Ray, Extraoral Source, Digital | MUH | 2 | Manufacturer | accessdata.fda.gov |
| Unit, Operative Dental, Accessories | NRD | 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 |
|---|---|---|---|---|---|---|
| March 3, 2026 | K251793 | SOTA Cloud Smart Sensor (1.5) | MUH | Substantially Equivalent | Sota Cloud Corp. | accessdata.fda.gov |
| May 4, 2021 | K210682 | SOTA Cloud Imaging | LLZ | Substantially Equivalent | Sota Precision Optics, Inc. Dba Sota Imaging | accessdata.fda.gov |
Compare with other makers
- All makers of System, Image Processing, Radiological
- All makers of Unit, Operative Dental, Accessories
- All makers of System, X-Ray, Extraoral Source, Digital
Updated March 3, 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.