Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3035544212

FEI Number

3035544212

Entity Name

WICKED SHEETS D/B/A WICKED TECHNOLOGIES

City/State/Country

Louisville, KY, US

Establishment Address

4217 Produce Rd, Louisville, KY 40218, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Wicked Sheets d/b/a Wicked Technologies (Owner Number: 10092711)

Owner / Operator Contact Address

4217 Produce Road, Louisville, KY 40218, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Wicked Smart Pad

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KPN	Alarm, Conditioned Response Enuresis	Gastroenterology, Urology	Class 2	876.2040	2025-02-08

Official Correspondent

Allison Truttmann

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Wicked Sheets d/b/a Wicked Technologies

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K780660	Nite Train-R Enterprises, Inc.	NITE TRAIN'R	1978-07-28
K871787	Dilorenzo Engineering Co.	ENURESIS ALARM	1987-08-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3035544212. Last updated year: 2026. Please use registration number 3035544212 when referencing this establishment in official correspondence.