Manufacturer registered with FDA

Tita-Link

Brussels, Belgium. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10031594Manufacturer

Device types listed: 1
Brands and models: 1
510(k) clearances: 12009–2009
Markets registered in: 1United States
Establishments: 1Belgium

510(k) clearances per year, 2000–2026

Devices listed with FDA

What Tita-Link 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	Bollard Mini Plates	2010

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 Tita-Link as the applicant, including filings under its other names.

Decided	510(k)	Device	Device type
8 Dec 2009	K091051	BOLLARD MINIPLATE SKELETAL ANCHORAGE SYSTEM	DZE Root-Form Endosseous Implant

Registered establishments

Establishment	Location	What it does
TITA-LINK B.V.B.AFDA reg. 3008252900	Brussels Brussels-Capital Region, Belgium	Manufacturer

Other names on FDA records

Tita-Link B.v.b.a

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10031594). 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.