Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2031447

FEI Number

3001890611

Entity Name

DR JOEL KAPLAN INC

City/State/Country

San Diego, CA, US

Establishment Address

3350 Market Street, Suite B, San Diego, CA 92102, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Dr Joel Kaplan Inc (Owner Number: 10083838)

Owner / Operator Contact Address

1220 Rosecrans Street, Suite 128, San Diego, CA 92106, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

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	2021-12-22

Official Correspondent

Judith Itshaki

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dr Joel Kaplan Inc

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

View Entity Profile →

Similar Registrations

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3023140863	FIRMTECH INC.	Bozeman, MT, US
3015200846	REACH MEDICAL, INC.	Collierville, TN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2031447. Last updated year: 2026. Please use registration number 2031447 when referencing this establishment in official correspondence.