Manufacturer registered with FDA

Magnum Medical

Chandler, AZ, United States. Lists 6 dental device types with FDA across 1 registered establishment.

FDA owner/operator1421307Repacker / relabelerSpecification developer
Device types listed
6
Brands and models
6
510(k) clearances
0as applicant
Markets registered in
32 registrations outside the US
Establishments
1United States

Registered in 3 markets

Where regulators' registries name Magnum Medical as the manufacturer or the registration holder of a device.

All markets
United States: 6 device types listedColombia: 1 registrationsSouth Korea: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerMagnum Medical6 device types—Below
ColombiaINVIMAManufacturerMAGNUM MEDICAL, INC.1—Pure Global AI
South KoreaMFDSManufacturerMagnum Medical12013–2013Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

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

Device typeCategoryRoleBrands and modelsListed since
Mouth MirrorEAX · Class 1Dental hand instrumentsLister
Dental Mirror
2022
Orthodontic Ligature Tucking InstrumentECP · Class 1Dental hand instrumentsLister
Ligature Tucking Instrument
2022
Dental Instrument HandleEJB · Class 1Dental hand instrumentsLister
Dental Handle
2022
Operative ExplorerEKB · Class 1Dental hand instrumentsLister
Dental Explorer
2022
Periodontic ScalerEMN · Class 1Dental hand instrumentsLister
Scaler Dental
2022
Orthodontic PlierJEX · Class 1Dental hand instrumentsMaker
Orthodontic Pliers
2023

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

Registered establishments

EstablishmentLocationWhat it does
MAGNUM MEDICAL, INC.FDA reg. 1421307CHANDLER, AZ, United StatesRepacker / relabeler, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 1421307). 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.