Silgan Unicep Packaging, LLC.

FDA Device Registration & Listing · Spokane, WA, US · Registration 1000150986

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
1000150986
FEI Number
3011913386
Entity Name
Silgan Unicep Packaging, LLC.
City/State/Country
Spokane, WA, US
Establishment Address
4122 S. Grove Road, Spokane, WA 99224, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Silgan Unicep (Owner Number: 10082972)
Owner / Operator Contact Address
1702 Industrial Drive, Sandpoint, ID 83864, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Zeltiq

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OOK Dermal Cooling Pack/Vacuum/Massager General, Plastic Surgery Class 2 878.4340 2021-10-18
GYB Media, Electroconductive Neurology Class 2 882.1275 2021-10-18

Official Correspondent

Steven Van Eps

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Silgan Unicep
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3028011 SILGAN UNICEP PACKAGING, LLC. SANDPOINT, ID, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000150986. Last updated year: 2026. Please use registration number 1000150986 when referencing this establishment in official correspondence.
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