Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1835058

FEI Number

1000517814

Entity Name

GLOBAL PLASTICS, INC.

City/State/Country

Indianapolis, IN, US

Establishment Address

6739 Guion Rd, Indianapolis, IN 46268, US

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Global Plastics, Inc. (Owner Number: 9020469)

Owner / Operator Contact Address

6739 GUION RD., --, Indianapolis, IN 46268, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

NeLLa Nuspec

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HIB	Speculum, Vaginal, Nonmetal	Obstetrics/Gynecology	Class 2	884.4530	2020-08-24

Official Correspondent

Micha Askelson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Global Plastics, Inc.

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 1835058. Last updated year: 2026. Please use registration number 1835058 when referencing this establishment in official correspondence.