Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012137049

FEI Number

3012137049

Entity Name

NELIPAK PHOENIX

City/State/Country

Phoenix, AZ, US

Establishment Address

3720 West Washington Street, Phoenix, AZ 85009, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Nelipak Phoenix (Owner Number: 10055012)

Owner / Operator Contact Address

3720 West Washington Street, Phoenix, AZ 85009, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Light Handle Cover

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FTA	Light, Surgical, Accessories	General, Plastic Surgery	Class 2	878.4580	2017-08-22

Official Correspondent

Rolando Salas

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nelipak Phoenix

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 3012137049. Last updated year: 2026. Please use registration number 3012137049 when referencing this establishment in official correspondence.