DRI VIEW

FDA Device Registration & Listing · Shepherdsville, KY, US · Registration 3010251578

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
3010251578
FEI Number
3010251578
Entity Name
DRI VIEW
City/State/Country
Shepherdsville, KY, US
Establishment Address
3214 E Blue Lick Rd, Shepherdsville, KY 40165, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Dri View (Owner Number: 10044348)
Owner / Operator Contact Address
3214 E Blue Lick Rd, Shepherdsville, KY 40165, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Revive

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LKY Device, External Penile Rigidity Gastroenterology, Urology Class 2 876.5020 2013-05-30

Official Correspondent

Jeff Durbin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010251578. Last updated year: 2026. Please use registration number 3010251578 when referencing this establishment in official correspondence.
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