Manufacturer registered with FDA

OsteoCentric Technologies Inc

Logan, UT, United States. Lists 2 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10049507Specification developer1 clearance in five years

Device types listed: 2
Brands and models: 2
510(k) clearances: 12023–2023
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 2007–2026

Devices listed with FDA

What OsteoCentric Technologies Inc currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Root-Form Endosseous ImplantDZE · Class 2	Dental implants	Maker	OsteoCentric Dental Implant System	2023
Endosseous Dental Implant AbutmentNHA · Class 2	Implant abutments	Maker	OsteoCentric Dental Implant System	2023

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 OsteoCentric Technologies Inc as the applicant.

Decided	510(k)	Device	Device type
5 Oct 2023	K230242	OsteoCentric Dental Implant System	DZE Root-Form Endosseous Implant

Registered establishments

Establishment	Location	What it does
OsteoCentric Technologies,IncFDA reg. 3011656326	Logan, UT, United States	Complaint file establishment, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10049507). 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.