Velentium Medical

FDA Device Registration & Listing · Richmond, TX, US · Registration 3014122529

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
3014122529
FEI Number
3014122529
Entity Name
Velentium Medical
City/State/Country
Richmond, TX, US
Establishment Address
7535 W Grand Pkwy S, Richmond, TX 77407, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Velentium (Owner Number: 10056737)
Owner / Operator Contact Address
7535 W Grand Parkway S, Richmond, TX 77407, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Sparrow Ascent System SealCath Double Balloon Rectal Catheter Vivistim System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PZR Percutaneous Nerve Stimulator For Opioid Withdrawal Neurology Class 2 882.5896 2023-11-17
FCE Enema Kit Gastroenterology, Urology Class 1 876.5210 2024-12-09
QPY Stimulator, Autonomic Nerve, Implanted For Stroke Rehabilitation Unknown Class 3 N/A 2023-11-17

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Velentium
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 3014122529. Last updated year: 2026. Please use registration number 3014122529 when referencing this establishment in official correspondence.
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