Manufacturer registered with FDA
Dti Implant Systems
KOCAELI, Türkiye. Lists 4 dental device types with FDA across 1 registered establishment.
- Device types listed
- 4
- Brands and models
- 4
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1Türkiye
Devices listed with FDA
What Dti Implant Systems currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Intraoral Dental DrillDZA · Class 1 | Surgical drills & motors | Maker | DTI | 2019 |
| Root-Form Endosseous ImplantDZE · Class 2 | Dental implants | Maker | DTI | 2019 |
| Endosseous Dental Implant AccessoriesNDP · Class 1 | Implant instruments & surgical kits | Maker | DTI | 2019 |
| Endosseous Dental Implant AbutmentNHA · Class 2 | Implant abutments | Maker | DTI | 2019 |
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
Dti Implant Systems 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: Dti Implant Sistemleri Sanayi Ticaret Anonim Sirketi (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 10 Apr 2018 | K170776 | DTI-1 SLA IMPLANT SYSTEM | Dti Implant Sistemleri Sanayi Ticaret Anonim Sirketi | DZE Root-Form Endosseous Implant |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| DTI IMPLANT SYSTEMSFDA reg. 3015218457 | Kocaeli, Türkiye | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10059446). 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.