VELMENI

FDA Device Registration & Listing · Sunnyvale, CA, US · Registration 3032960222

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3032960222
FEI Number
3032960222
Entity Name
VELMENI
City/State/Country
Sunnyvale, CA, US
Establishment Address
333 W Maude Ave Ste 207, Sunnyvale, CA 94085, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Velmeni (Owner Number: 10091698)
Owner / Operator Contact Address
333 W. Maude Ave #207, Sunnyvale, CA 94085, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

3D Verify

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LHO Instrument, Quality-Assurance, Radiologic Radiology Class 1 892.1940 2025-03-21

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Velmeni
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032960222. Last updated year: 2026. Please use registration number 3032960222 when referencing this establishment in official correspondence.
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