Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021520400

FEI Number

3021520400

Entity Name

RAPIDPULSE, INC.

City/State/Country

Miami, FL, US

Establishment Address

13755 SW 119th Avenue, Miami, FL 33186, US

Establishment Type(s)

Manufacture Device in the United States for Export Only

Owner / Operator

RapidPulse, Inc. (Owner Number: 10084870)

Owner / Operator Contact Address

14250 SW 119th Avenue, Miami, FL 33186, 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
NRY	Catheter, Thrombus Retriever	Cardiovascular	Class 2	870.1250	2022-04-08

Official Correspondent

Heather Harries

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RapidPulse, Inc.

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
K033736	Concentric Medical, Inc.	MERCI RETRIEVER, MODELS 90065, 90066	2004-08-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021520400. Last updated year: 2026. Please use registration number 3021520400 when referencing this establishment in official correspondence.