MOXI ENTERPRISES, LLC

FDA Device Registration & Listing · Greenville, SC, US · Registration 3008146946

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
3008146946
FEI Number
3008146946
Entity Name
MOXI ENTERPRISES, LLC
City/State/Country
Greenville, SC, US
Establishment Address
1927 Perimeter Road, Unit B, Greenville, SC 29605, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Moxi Enterprises (Owner Number: 10031033)
Owner / Operator Contact Address
1927 Perimeter Road, Unit B, Greenville, SC 29605, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Fusion Fusion SelectAir BariSelect ProtectYou2 Fusion SelectAir

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKY Mattress, Flotation Therapy, Non-Powered General Hospital Class 1 880.5150 2019-05-23
FNM Mattress, Air Flotation, Alternating Pressure General Hospital Class 2 880.5550 2009-12-11
FMW Cover, Mattress (Medical Purposes) General Hospital Class 1 880.6190 2022-11-07

Official Correspondent

Dale Thomas

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Similar Registrations

Registration Number Establishment Name Location
3008775647 SHAKAM, LLC Columbus, OH, US
3018115503 COMFORT CARE PRODUCTS, LLC Newberry, SC, US
3032847786 Cutters Foam Fabricating, Inc. Elkhart, IN, US
3004116007 Legs 4 Life, LLC ASHEBORO, NC, US
3009056001 STME Acquisition LLC Palmetto, GA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008146946. Last updated year: 2026. Please use registration number 3008146946 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.