ANUNCIA MEDICAL, INC.

FDA Device Registration & Listing · Scottsdale, AZ, US · Registration 3014522419

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014522419
FEI Number
3014522419
Entity Name
ANUNCIA MEDICAL, INC.
City/State/Country
Scottsdale, AZ, US
Establishment Address
6908 E Thomas Rd Ste 302, Scottsdale, AZ 85251, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Anuncia Medical (Owner Number: 10057485)
Owner / Operator Contact Address
6908 E Thomas Road, Suite 302, Scottsdale, AZ 85251, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

ReFlow System Mini and ReFlow Mini Flusher

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JXG Shunt, Central Nervous System And Components Neurology Class 2 882.5550 2023-02-16

Official Correspondent

Elsa Abruzzo

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Anuncia Medical
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
K981246 Integra Neurocare, LLC BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER (NL850-9720) VALVE KIT (NL850-9730) 1999-05-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014522419. Last updated year: 2026. Please use registration number 3014522419 when referencing this establishment in official correspondence.
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