Registered with FDA

Masterlink, LLC.

Peoria, AZ, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10054572Repacker / relabeler
Device types listed
1
Brands and models
2
510(k) clearances
12017–2017
Markets registered in
1United States
Establishments
1United States
2017: 120102020

510(k) clearances per year, 2007–2026

Devices listed with FDA

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

Device typeCategoryRoleBrands and modelsListed since
Digital Extraoral Source X-Ray SystemMUH · Class 2Dental X-ray unitsLister
Apex Dental Sensor 1Apex Dental Sensor 2
2017

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 Masterlink, LLC. as the applicant.

Decided510(k)DeviceDevice type
28 Feb 2017K163282Apex Dental SensorsMUH Digital Extraoral Source X-Ray System

Registered establishments

EstablishmentLocationWhat it does
MASTERLINK, LLC.FDA reg. 3013651568Peoria, AZ, United StatesComplaint file establishment, Repacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10054572). 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.