DUCT-AID

FDA Device Registration & Listing · Cedar City, UT, US · Registration 3015545156

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
3015545156
FEI Number
3015545156
Entity Name
DUCT-AID
City/State/Country
Cedar City, UT, US
Establishment Address
2086 N Ashdown Forest Rd, Cedar City, UT 84721, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Duct-Aid (Owner Number: 10094338)
Owner / Operator Contact Address
2086 N Ashdown Forest Road, Cedar City, UT 84721, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Duct Aid Duct Tape

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PYO Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use General Hospital Class 1 880.5240 2025-11-24

Official Correspondent

Wade Melling

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Duct-Aid
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 3015545156. Last updated year: 2026. Please use registration number 3015545156 when referencing this establishment in official correspondence.
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