Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010832019

FEI Number

3010832019

Entity Name

RX SLEEVE

City/State/Country

Upland, CA, US

Establishment Address

1525 W 13th St Ste C, Upland, CA 91786, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

RX Sleeve (Owner Number: 10046623)

Owner / Operator Contact Address

1525 W. 13th Street., Suite C, Upland, CA 91786, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

KONA MAUI MANHATTAN BALBOA PALM SURFSIDE HERMOSA PERFECT CORONA KNIGHT MISSION

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	2014-04-16

Official Correspondent

Natalie Tomlinson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RX Sleeve

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 3010832019. Last updated year: 2026. Please use registration number 3010832019 when referencing this establishment in official correspondence.