Data / Medical devices / United States / Medwand Solutions, Inc
Medwand Solutions, Inc: FDA-registered device maker in Rsm, CA, United States, 1 510(k) clearance
Medwand Solutions, Inc is registered with the FDA (registration 3024491912) in Rsm, CA, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 22, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3024491912
- Address
- 23162 Arroyo Vista, Rsm, CA, United States, 92688
- Owner or operator
- MedWand Solutions, Inc (10086016)
- Roles
- Specification developer
- First device listed
- October 10, 2022
- Registered through
- 2026
- Brand names listed
- MedWand (tm) Device
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Continuous Measurement Thermometer | FLL | 2 | Specification developer | accessdata.fda.gov |
| Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) | MWI | 2 | Specification developer | accessdata.fda.gov |
| Oximeter | DQA | 2 | Specification developer | accessdata.fda.gov |
| Stethoscope, Electronic | DQD | 2 | Specification developer | 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 22, 2022 | K212975 | MedWand | MWI | Substantially Equivalent | Medwand Solutions, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Oximeter
- All makers of Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
- All makers of Stethoscope, Electronic
- All makers of Continuous Measurement Thermometer
Updated July 22, 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.