Remvia, LLC

FDA Device Registration & Listing · Saint Louis, MO, US · Registration 3043044356

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
3043044356
FEI Number
3043044356
Entity Name
Remvia, LLC
City/State/Country
Saint Louis, MO, US
Establishment Address
911 Washington Ave Ste 500, Saint Louis, MO 63101, US
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Founder (Owner Number: 10095000)
Owner / Operator Contact Address
8403 w. Buckskin Rd, Pocatello, ID 83201, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K250743
PMA Number
N/A

All Registered Proprietary Names

Remvia Night Guard

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OCO Mouthguard, Migraine/Tension Headache Unknown Class U N/A 2026-01-13
MQC Mouthguard, Prescription Unknown Class U N/A 2026-01-13

Official Correspondent

Nephi Zufelt

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Founder
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 3043044356. Last updated year: 2026. Please use registration number 3043044356 when referencing this establishment in official correspondence.
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