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Data / Medical devices / United States / PRENUVO Inc.

PRENUVO Inc.: FDA-registered device maker in Redwood City, CA, United States, 1 510(k) clearance

PRENUVO Inc. is registered with the FDA (registration 3017297314) in Redwood City, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 17, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3017297314
Address
2727 El Camino Real, Redwood City, CA, United States, 94061
Owner or operator
Prenuvo (10092617)
Roles
Manufacturer
First device listed
January 29, 2025
Registered through
2026
Brand names listed
PRENUVO BODY COMPOSITION

Devices it lists

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 17, 2025K242825Prenuvo Body CompositionLNHSubstantially EquivalentPrenuvoaccessdata.fda.gov

Compare with other makers

Updated January 17, 2025. 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.