RITEWIPE

FDA Device Registration & Listing · Cheyenne, WY, US · Registration 3030856996

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
3030856996
FEI Number
3030856996
Entity Name
RITEWIPE
City/State/Country
Cheyenne, WY, US
Establishment Address
1620 Central Ave Rm 204, Cheyenne, WY 82001, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
RiteWipe (Owner Number: 10090619)
Owner / Operator Contact Address
1620 Central Ave, Rm 204, Cheyenne, WY 82001, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

RiteWipe Handpiece Wipe

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRJ Disinfectant, Medical Devices General Hospital Class 1 880.6890 2024-04-19

Official Correspondent

Brandon Baker

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RiteWipe
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 3030856996. Last updated year: 2026. Please use registration number 3030856996 when referencing this establishment in official correspondence.
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