PD PRODUCTS LLC

FDA Device Registration & Listing · West Hills, CA, US · Registration 3010849337

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
3010849337
FEI Number
3010849337
Entity Name
PD PRODUCTS LLC
City/State/Country
West Hills, CA, US
Establishment Address
8521 Fallbrook Ave Ste 380, West Hills, CA 91304, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
PD Products, LLC (Owner Number: 10058698)
Owner / Operator Contact Address
8501 Fallbrook Ave Suite #370, West Hills, CA 91304, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pipedream Beginner's Power Pump - Blue - 324114 Pump Worx Beginner's Power Pump - Purple - 326012 Pump Worx Max Boost - Black - 324923 Pump Worx Rookie of the Year Pump - Clear/Black - 325323 Pipedream Beginner's Power Pump - Black - 324124 Pump Worx Max-Width Penis Enlarger - Clear/Black - 326223 Pump Worx Accu-Meter Power Pump - Clear/Black - 327223 Pump Worx Beginner's Power Pump - Red - 326015 Pump Worx Silicone Power Pump - Clear/Black - 325520 Classix Vibrating Power Pump - Clear, 192700 Pump Worx Beginner's Power Pump - Smoke/Black - 326023 Pump Worx Beginner's Power Pump - Blue - 326014 Pump Worx Pistol-Grip Power Pump - Clear/Black - 326623 Pump Worx Silicone Power Pump - Blue - 325514 Pump Worx Beginner's Vibrating Pump - Clear/Black - 325023 Pump Worx Max Boost - Blue - 324925 Max Boost Pro Flow - Blue/Clear - 325025 Max Boost Pro Flow - White/Clear - 325019 Pump Worx Max Boost - White - 324919 Classix Power Pump, 190800 Pipedream Beginner's Power Pump - Clear - 324120 Pump Worx Beginner's Power Pump - Clear - 326020

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 2023-10-16

Official Correspondent

Hermine Zanki

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PD Products, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010849337. Last updated year: 2026. Please use registration number 3010849337 when referencing this establishment in official correspondence.
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