RALLINSON CORP

FDA Device Registration & Listing · Miami, FL, US · Registration 3027486037

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
3027486037
FEI Number
3027486037
Entity Name
RALLINSON CORP
City/State/Country
Miami, FL, US
Establishment Address
111 NE 1st St, 8th Floor Suite 88417, Miami, FL 33132, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Rallinson Corp (Owner Number: 10088174)
Owner / Operator Contact Address
111 NE 1st St, 8th Floor Suite 88417, Miami, FL 33132, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Testic Breast Check WoundSkan ThermaDerm Footflow

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FQZ Thermometer, Clinical Color Change General Hospital Class 1 880.2900 2023-06-06

Official Correspondent

Jack Kaye

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Rallinson Corp
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027486037. Last updated year: 2026. Please use registration number 3027486037 when referencing this establishment in official correspondence.
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