GLOBAL SOURCE RX

FDA Device Registration & Listing · Scottsdale, AZ, US · Registration 3010539382

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
3010539382
FEI Number
3010539382
Entity Name
GLOBAL SOURCE RX
City/State/Country
Scottsdale, AZ, US
Establishment Address
14505 North Hayden Road, suite 101, Scottsdale, AZ 85260, US
Establishment Type(s)
Reprocess Single-Use Device,Repack or Relabel Medical Device
Owner / Operator
Global Source RX (Owner Number: 10045411)
Owner / Operator Contact Address
14505 North Hayden Road, suite 101, Scottsdale, AZ 85260, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Epik Single Vision Epik Lenses Epik Standard Epik Day Epik Office Epik Variable

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2015-02-06

Official Correspondent

Keith Posin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Global Source RX
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 3010539382. Last updated year: 2026. Please use registration number 3010539382 when referencing this establishment in official correspondence.
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