INTERTEK INDUSTRIAL CORP

FDA Device Registration & Listing · Jacksonville, FL, US · Registration 3005822866

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
3005822866
FEI Number
3005822866
Entity Name
INTERTEK INDUSTRIAL CORP
City/State/Country
Jacksonville, FL, US
Establishment Address
3023 Powers Ave, Jacksonville, FL 32207, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Intertek Industrial Corp (Owner Number: 10043302)
Owner / Operator Contact Address
3023 Powers Ave, Jacksonville, FL 32207, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NZD Stretcher, Patient Restraint General Hospital Class 1 880.6900 2013-07-16

Official Correspondent

Scott Bradley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Intertek Industrial 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 3005822866. Last updated year: 2026. Please use registration number 3005822866 when referencing this establishment in official correspondence.
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