InterMetro de Acuna

FDA Device Registration & Listing · Acuna Coahuila, MX · Registration 3009526986

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
3009526986
FEI Number
3009526986
Entity Name
InterMetro de Acuna
City/State/Country
Acuna Coahuila, MX
Establishment Address
Calle Zacatecas 505, Parque Industrial Amistad, Acuna Coahuila 26220, MX
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
INTERMETRO INDUSTRIES CORP. (Owner Number: 9020459)
Owner / Operator Contact Address
651 NORTH WASHINGTON ST., --, Wilkes Barre, PA 18705, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Flexline Anesthesia Cart Starsys Anesthesia Cart LEC Backboard Lifeline Code Response Cart Flexline Code Response Cart

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SEU Peripheral Temporary And Retrievable Stent System Cardiovascular Class 2 870.5110 2025-11-24
BRY Cabinet, Table And Tray, Anesthesia Anesthesiology Class 1 868.6100 1996-09-09
FOA Board, Cardiopulmonary General Hospital Class 1 880.6080 2020-12-02
BZN Cart, Emergency, Cardiopulmonary (Excluding Equipment) Anesthesiology Class 1 868.6175 2005-05-03

Official Correspondent

Rocky Selenski

US Agent Details

Rocky Selenski Business: InterMetro Industries Corporation Email: rocky.selenski@metro.com Phone: (570) 7064354

Related Public Records

Same Entity

INTERMETRO INDUSTRIES CORP.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
2531463 INTERMETRO INDUSTRIES CORP Wilkes Barre, PA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009526986. Last updated year: 2026. Please use registration number 3009526986 when referencing this establishment in official correspondence.
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