INTERMETRO INDUSTRIES CORP

FDA Device Registration & Listing · Wilkes Barre, PA, US · Registration 2531463

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
2531463
FEI Number
3001600991
Entity Name
INTERMETRO INDUSTRIES CORP
City/State/Country
Wilkes Barre, PA, US
Establishment Address
651 NORTH WASHINGTON ST., --, Wilkes Barre, PA 18705, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
INTERMETRO INDUSTRIES CORP. (Owner Number: 9020459)
Owner / Operator Contact Address
651 NORTH WASHINGTON ST., --, Wilkes Barre, PA 18705, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Flexline Anesthesia Cart Starsys Anesthesia Cart 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
BZN Cart, Emergency, Cardiopulmonary (Excluding Equipment) Anesthesiology Class 1 868.6175 2005-05-03

Official Correspondent

Rocky Selenski

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

INTERMETRO INDUSTRIES CORP.
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 2531463. Last updated year: 2026. Please use registration number 2531463 when referencing this establishment in official correspondence.
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