Data / Medical devices / United States / Menlo Brands
Menlo Brands: FDA-registered device maker in Menlo Park, CA, United States, 1 510(k) clearance
Menlo Brands is registered with the FDA (registration 3015228371) in Menlo Park, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 19, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015228371
- Address
- 2045 Avy Avenue, Menlo Park, CA, United States, 94025
- Owner or operator
- Menlo Brands (10061805)
- Roles
- Specification developer
- First device listed
- November 20, 2019
- Registered through
- 2026
- Brand names listed
- Speed Hound ProPerformance Recovery System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Powered Inflatable Tube | IRP | 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 |
|---|---|---|---|---|---|---|
| September 19, 2019 | K192252 | ProPerformance Recovery System | IRP | Substantially Equivalent | Menlo Brands, LLC | accessdata.fda.gov |
Compare with other makers
Updated September 19, 2019. 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.