Manufacturer registered with FDA

Armm, Inc.

Huntington Beach, CA, United States. Lists 4 dental device types with FDA across 1 registered establishment.

FDA owner/operator9005125Contract manufacturerContract sterilizer
Device types listed
4
Brands and models
1
510(k) clearances
0as applicant
Markets registered in
32 registrations outside the US
Establishments
1United States

Registered in 3 markets

Where regulators' registries name Armm, Inc. as the manufacturer or the registration holder of a device.

All markets
United States: 4 device types listedBrazil: 1 registrationsTaiwan: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerArmm, Inc.4 device types—Below
BrazilANVISAManufacturerARMM INC.12011–2011Pure Global AI
TaiwanTFDAManufacturerARMM, INC.12011–2011Pure 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 Armm, Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Hand InstrumentsDZN · Class 1Dental hand instrumentsMaker—2013
Dental Surgical ElevatorEMJ · Class 1Dental hand instrumentsMaker—2013
Periodontic FileEMR · Class 1Dental hand instrumentsMaker
Subantral Membrane Elevators
2009
Intraoral Animal Source BarrierNPL · Class 2Bone grafts & membranesMaker—2013

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
ARMM, INC.FDA reg. 2028523HUNTINGTON BEACH, CA, United StatesContract manufacturer, Contract sterilizer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9005125). 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.