ALPEP LLC

FDA Device Registration & Listing · Orange, CA, US · Registration 3023230882

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
3023230882
FEI Number
3023230882
Entity Name
ALPEP LLC
City/State/Country
Orange, CA, US
Establishment Address
1547 W. Struck Ave., Suite G, Orange, CA 92867, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AlPep LLC (Owner Number: 10085596)
Owner / Operator Contact Address
1547 W. Struck Ave.,, Suite G, Orange, CA 92867, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

UniSUC WHISPER

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NNZ System, Urine Drainage, Closed, For Non-Indwelling Catheter, Non-Sterile Gastroenterology, Urology Class 1 876.5250 2025-03-01

Official Correspondent

Allan Pepito

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AlPep LLC
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 3023230882. Last updated year: 2026. Please use registration number 3023230882 when referencing this establishment in official correspondence.
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