Data / Medical devices / United States / Foxx Development Inc.
Foxx Development Inc.: FDA-registered device maker in Alpharetta, GA, United States, 4 510(k) clearances
Foxx Development Inc. is registered with the FDA (registration 3032948391) in Alpharetta, GA, United States. It lists 6 device types. The FDA files 4 510(k) clearances under its listings, the newest dated March 20, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3032948391
- Address
- 3480 Preston Ridge Rd Ste 500, Alpharetta, GA, United States, 30005
- Owner or operator
- Foxx Development Inc. (10091595)
- Roles
- Repackager or relabeler
- First device listed
- November 5, 2024
- Registered through
- 2026
- Brand names listed
- BFS1, Blood Glucose Meter, Bluetooth body fat scale, ECG Smart ring: R1E, EYE MASSAGER, Fingertip Pulse Oximeter, INFRARED THERMOMETER, MB1 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Body Composition, Exempt | PUH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Oximeter | DQA | 2 | Repackager or relabeler | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Repackager or relabeler | accessdata.fda.gov |
| System, Test, Blood Glucose, Over The Counter | NBW | 2 | 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 |
|---|---|---|---|---|---|---|
| March 20, 2020 | K191657 | Bioland Blood Glucose Monitoring System | NBW | Substantially Equivalent | Bioland Technology, Ltd. | accessdata.fda.gov |
| May 8, 2017 | K161938 | Fingertip Pulse Oximeter | DQA | Substantially Equivalent | Xuzhou Yongkang Electronic Science Technology Co., Ltd. | accessdata.fda.gov |
| August 21, 2014 | K140681 | BELTER INFRA-RED EAR THERMOMETER | FLL | Substantially Equivalent | Shenzhen Belter Health Measurement and Analysis TE | accessdata.fda.gov |
| July 25, 2014 | K134029 | BELTER BLOOD PRESSURE METER | DXN | Substantially Equivalent | Shenzhen Belter Health Measurement and Analysis TE | accessdata.fda.gov |
Compare with other makers
- All makers of Oximeter
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Analyzer, Body Composition, Exempt
- All makers of System, Test, Blood Glucose, Over The Counter
- All makers of Continuous Measurement Thermometer
- All makers of Massager, Therapeutic, Electric
Updated March 20, 2020. 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.