Data / Medical devices / United States / Veris Health
Veris Health: FDA-registered device maker in Foxborough, MA, United States, 3 510(k) clearances
Veris Health is registered with the FDA (registration 3026585241) in Foxborough, MA, United States. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 29, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3026585241
- Address
- 200 Foxborough Boulevard Suite 300, Foxborough, MA, United States, 02035
- Owner or operator
- Veris Health (10086341)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- February 21, 2023
- Registered through
- 2026
- Brand names listed
- Veris Health Cancer Care Platform
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Continuous Measurement Thermometer | FLL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Medical Device Data System | OUG | 1 | Specification developer | 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 |
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 29, 2022 | K220676 | Blood Pressure Monitor | DXN | Substantially Equivalent | Guangdong Transtek Medical Electronics Co., Ltd. | accessdata.fda.gov |
| December 7, 2020 | K202173 | Pulse Oximeter | DQA | Substantially Equivalent | Shenzhen AOJ Medical Technology Co., Ltd. | accessdata.fda.gov |
| November 20, 2018 | K182133 | Infrared Thermometer | FLL | Substantially Equivalent | Shenzhen AOJ Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Oximeter
- All makers of Medical Device Data System
- All makers of Continuous Measurement Thermometer
Updated August 29, 2022. 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.