Manufacturer registered with FDA

Louisiana Dental Implant Lab

Lafayette, LA, United States. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator10090364Contract manufacturerSpecification developer
Device types listed
2
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What Louisiana Dental Implant Lab currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Root-Form Endosseous ImplantDZE · Class 2Dental implantsMaker
Vortex
2024
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsMaker
abutment, implant, dental, endosseous
2024

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

Also lists devices cleared under other names

Louisiana Dental Implant Lab lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.

Original applicants: The Emerging Technologies Group (1).

Decided510(k)DeviceApplicantDevice type
25 Sep 1996K961384MT-2The Emerging Technologies GroupDZE Root-Form Endosseous Implant

Registered establishments

EstablishmentLocationWhat it does
LOUISIANA DENTAL IMPLANT LABFDA reg. 3020144887Lafayette, LA, United StatesContract manufacturer, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10090364). 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.