REZZIMAX, LLC

FDA Device Registration & Listing · Smithfield, UT, US · Registration 3033407717

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
3033407717
FEI Number
3033407717
Entity Name
REZZIMAX, LLC
City/State/Country
Smithfield, UT, US
Establishment Address
489 S 620 E, Smithfield, UT 84335, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Rezzimax, LLC (Owner Number: 10091700)
Owner / Operator Contact Address
489 S 620 E, Smithfield, UT 84335, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Rezzimax Mini Rezzimax Tuner

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IRO Vibrator, Therapeutic Physical Medicine Class 1 890.5975 2024-10-24

Official Correspondent

Sharik Peck

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K821133 Durham Electric Co. ELECTRICAL VIBRATING DEVICE 1982-07-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033407717. Last updated year: 2026. Please use registration number 3033407717 when referencing this establishment in official correspondence.
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