Manufacturer registered with FDA

Oral Arts Laboratory, Inc.

Huntsville, AL, United States. Lists 3 dental device types with FDA across 1 registered establishment.

FDA owner/operator10039789Contract manufacturer
Device types listed
3
Brands and models
9
510(k) clearances
0as applicant
Markets registered in
233 registrations outside the US
Establishments
1United States

Registered in 2 markets

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

All markets
United States: 3 device types listedUnited Kingdom: 33 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerOral Arts Laboratory, Inc.3 device types—Below
United KingdomMHRAManufacturerOral Arts Laboratory Ltd33—Pure 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 Oral Arts Laboratory, Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Anti-Snoring DeviceLRK · Class 2Anti-snoring & jaw-repositioning devicesMaker
EMAEMA 3DQuietNiteTAP III
2012
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsMaker
Abutment, Implant, Dental, Endosseous-Keystone AbutmentsAbutment, Implant, Dental, Endosseous-Preat AbutmentsAbutment, Implant, Dental, Endosseous, Biodenta Customize Abutment-HybridAbutment, Implant, Dental. Endosseous,-Biodenta Customized Abutment-Titanium
2020
Jaw Repositioning DeviceLQZ · Class 2Anti-snoring & jaw-repositioning devicesMaker
EMA 3D
2025

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
Oral Arts Laboratory, Inc.FDA reg. 3005730680Huntsville, AL, United StatesContract manufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10039789). 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.