REMEDY MEDICAL MANUFACTURING

FDA Device Registration & Listing · Mesa, AZ, US · Registration 3015865915

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
3015865915
FEI Number
3015865915
Entity Name
REMEDY MEDICAL MANUFACTURING
City/State/Country
Mesa, AZ, US
Establishment Address
2260 W Broadway Rd Ste 101, Mesa, AZ 85202, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Remedy Medical Manufacturing (Owner Number: 10061246)
Owner / Operator Contact Address
2260 W Broadway Rd, STE 101, Mesa, AZ 85202, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

StomaEase ReFlow® System Mini, ReFlow® Mini Flusher EsophaCap

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EXB Collector, Ostomy Gastroenterology, Urology Class 1 876.5900 2024-05-13
JXG Shunt, Central Nervous System And Components Neurology Class 2 882.5550 2023-06-30
EOX Esophagoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4710 2019-10-03

Official Correspondent

David Szabo

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Remedy Medical Manufacturing
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

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2012 Convatec Inc. 1
Natura Durahesive ConvaTec Moldable Technology Post-Operative /Surgical System (57 mm) Required for application to a patient immediately after ostomy surgery.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015865915. Last updated year: 2026. Please use registration number 3015865915 when referencing this establishment in official correspondence.
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