Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017128979

FEI Number

3017128979

Entity Name

CRC EP, INC.

City/State/Country

Tustin, CA, US

Establishment Address

3002 Dow Avenue, Suite 526, Tustin, CA 92780, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

CRC EP, Inc. (Owner Number: 10087123)

Owner / Operator Contact Address

3002 Dow Avenue, Suite 526, Tustin, CA 92780, 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
OAE	Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation	Unknown	Class 3	N/A	2023-01-14

Official Correspondent

Dorin Panescu

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CRC EP, Inc.

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 3017128979. Last updated year: 2026. Please use registration number 3017128979 when referencing this establishment in official correspondence.