Data / Medical devices / United States / XRD Dental Equipment
XRD Dental Equipment: FDA-registered device maker in Clermont, FL, United States, 1 510(k) clearance
XRD Dental Equipment is registered with the FDA (registration 3015153900) in Clermont, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 13, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015153900
- Address
- 16991 Cedar Valley Cir, Clermont, FL, United States, 34711
- Owner or operator
- XRD Dental Equipment (10062060)
- Roles
- Complaint file establishment
- First device listed
- July 25, 2023
- Registered through
- 2026
- Brand names listed
- XRD RAY98(P)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Unit, X-Ray, Extraoral With Timer | EHD | 2 | Complaint file establishment | 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 |
|---|---|---|---|---|---|---|
| July 13, 2023 | K231449 | Portable X-ray System Model Ray98(P) | EHD | Substantially Equivalent | Ningbo Runyes Medical Instrument Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 13, 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.