RADIUM INCORPORATED

FDA Device Registration & Listing · Waynesboro, VA, US · Registration 3020824984

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
3020824984
FEI Number
3020824984
Entity Name
RADIUM INCORPORATED
City/State/Country
Waynesboro, VA, US
Establishment Address
463 Dinwiddie Ave., Waynesboro, VA 22980, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Radium Incorporated (Owner Number: 10084949)
Owner / Operator Contact Address
463 Dinwiddie Ave., Waynesboro, VA 22980, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ClearView Syringe Shield ClearView Vial Shield

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IWR Holder, Syringe, Lead Radiology Class 1 892.6500 2022-11-28
IWW Shield, Vial Radiology Class 1 892.6500 2022-04-27

Official Correspondent

Cam Abernethy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Radium Incorporated
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 3020824984. Last updated year: 2026. Please use registration number 3020824984 when referencing this establishment in official correspondence.
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