Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027098402

FEI Number

3027098402

Entity Name

RENATA MEDICAL

City/State/Country

Newport Beach, CA, US

Establishment Address

4675 Macarthur Ct Ste 1150, Newport Beach, CA 92660, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Renata Medical (Owner Number: 10089373)

Owner / Operator Contact Address

4675 MacArthur Ct, 1150, Newport Beach, CA 92660, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P240003

All Registered Proprietary Names

Minima Stent System Minima System Minima Stent Minima Growth Stent Minima

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PNF	Aortic Stent	Unknown	Class 3	N/A	2024-08-30
QWC	Pulmonary Stent	Unknown	Class 3	N/A	2024-08-30

Official Correspondent

Ben Krebs

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Renata Medical

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 3027098402. Last updated year: 2026. Please use registration number 3027098402 when referencing this establishment in official correspondence.