Manufacturer registered with FDA

Aiomega, LLC

Tyler, TX, United States. Lists 2 dental device types with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.

FDA owner/operator10090223Manufacturer2 clearances in five years

Device types listed: 2
Brands and models: 2
510(k) clearances: 22024–2025
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 2007–2026

Devices listed with FDA

What Aiomega, LLC currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Jaw Repositioning DeviceLQZ · Class 2	Anti-snoring & jaw-repositioning devices	Maker	AIO BREATHE	2024
Anti-Snoring DeviceLRK · Class 2	Anti-snoring & jaw-repositioning devices	Maker	AIO BREATHE	2024

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names Aiomega, LLC as the applicant.

Decided	510(k)	Device	Device type
6 Nov 2025	K252525	AIO Breathe	LRK Anti-Snoring Device
23 Feb 2024	K233754	AIO Breathe	LQZ Jaw Repositioning Device

Registered establishments

Establishment	Location	What it does
AIOMEGA, LLCFDA reg. 3030562551	Tyler, TX, United States	Manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10090223). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.