RAMPART IC, Inc

FDA Device Registration & Listing · Birmingham, AL, US · Registration 3038966231

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
3038966231
FEI Number
3038966231
Entity Name
RAMPART IC, Inc
City/State/Country
Birmingham, AL, US
Establishment Address
101 Shades Creek Cir Ste C, Birmingham, AL 35211, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Rampart Inc. (Owner Number: 10062102)
Owner / Operator Contact Address
1500 Urban Center Drive Ste 140, Birmingham, AL 35242, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Rampart Radiation Head Shield RHS-01 Rampart IC Defender M1128-RTV Radiation Shield Right Table Version Rampart IC Sentry Mobile Radiation Shield P1442-SMS Rampart IC Guardian Radiation Shield M1130-TPS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EAK Screen, Leaded, Operator Radiation Protector Radiology Class 1 892.6500 2019-12-18

Official Correspondent

Jane Rodd

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3016257387 RAMPART IC, Inc Birmingham, AL, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038966231. Last updated year: 2026. Please use registration number 3038966231 when referencing this establishment in official correspondence.
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