Data / Medical devices / United States / DR. Noze Best
DR. Noze Best: FDA-registered device maker in Atlanta, GA, United States, 1 510(k) clearance
DR. Noze Best is registered with the FDA (registration 3017973191) in Atlanta, GA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 19, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017973191
- Address
- 235 Mitchell St SW Ste 285, Atlanta, GA, United States, 30303
- Owner or operator
- Dr. Noze Best (10079863)
- Roles
- Complaint file establishment, Repackager or relabeler, Specification developer
- First device listed
- December 31, 2020
- Registered through
- 2026
- Brand names listed
- Dr. Noze Best Nebulizer, NEBU-001, Dr. Noze Best Thermometer, DNBT-001, NozeBot Nasal Aspirator, NozeBot On the Go Nasal Aspirator
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bottle, Collection, Vacuum | KDQ | 2 | Complaint file establishment, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Complaint file establishment, Repackager or relabeler | accessdata.fda.gov |
| Nebulizer, Medicinal, Non-Ventilatory (Atomizer) | CCQ | 1 | Complaint file establishment, Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| April 19, 2018 | K172427 | AViTA Radar Thermo NT16 Series IR Thermometer | FLL | Substantially Equivalent | Avita Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Bottle, Collection, Vacuum
- All makers of Continuous Measurement Thermometer
- All makers of Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Updated April 19, 2018. 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.