UNIPACK LLC

FDA Device Registration & Listing · Pittsburgh, PA, US · Registration 2522811

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
2522811
FEI Number
2522811
Entity Name
UNIPACK LLC
City/State/Country
Pittsburgh, PA, US
Establishment Address
3249 Old Frankstown Rd., Pittsburgh, PA 15239, US
Establishment Type(s)
Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Unipack LLC (Owner Number: 10086036)
Owner / Operator Contact Address
3249 Old Frankstown Rd., Pittsburgh, PA 15239, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Menthol Nasal Inhaler

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KCO Nasal Spray, Ent Delivery Ear, Nose, Throat Class 1 874.5220 2022-10-12

Official Correspondent

Dinesh Patel

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Unipack LLC
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 2522811. Last updated year: 2026. Please use registration number 2522811 when referencing this establishment in official correspondence.
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