Data / Medical devices / United States / Rva Medical LLC
Rva Medical LLC: FDA-registered device maker in Aylett, VA, United States, 1 510(k) clearance
Rva Medical LLC is registered with the FDA (registration 3033332986) in Aylett, VA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 14, 2021. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3033332986
- Address
- 52 Fairmont Pl, Aylett, VA, United States, 23009
- Owner or operator
- RVA Medical LLC (10091857)
- Roles
- Repackager or relabeler
- First device listed
- November 7, 2024
- Registered through
- 2026
- Brand names listed
- MY-123, MY-123-1
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Nebulizer (Direct Patient Interface) | CAF | 2 | Repackager or relabeler | accessdata.fda.gov |
| Nebulizer, Medicinal, Non-Ventilatory (Atomizer) | CCQ | 1 | 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 |
|---|---|---|---|---|---|---|
| June 14, 2021 | K201397 | Ultrasonic Mesh Nebulizer | CAF | Substantially Equivalent | Shenzhen Ivankaca Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Nebulizer (Direct Patient Interface)
- All makers of Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Updated June 14, 2021. 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.