Manufacturer registered with FDA
Titan Implants, Inc.
Bergenfield, NJ, United States. Lists 3 dental device types with FDA across 1 registered establishment, and holds 4 510(k) clearances as applicant.
- Device types listed
- 3
- Brands and models
- 3
- 510(k) clearances
- 42001–2005
- Markets registered in
- 1United States
- Establishments
- 1United States
510(k) clearances per year, 2000–2026
Devices listed with FDA
What Titan Implants, 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 | TITAN IMPLANTS | 2000 |
| Endosseous Dental Implant AccessoriesNDP · Class 1 | Implant instruments & surgical kits | Maker | TITAN IMPLANTS, INC. | 2016 |
| Endosseous Dental Implant AbutmentNHA · Class 2 | Implant abutments | Maker | Titan Implants | 2014 |
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 Titan Implants, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 23 Mar 2005 | K042715 | TITAN DENTAL IMPLANT ATTACHMENT | NHA Endosseous Dental Implant Abutment |
| 14 Jan 2005 | K042971 | TITAN DENTAL IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 4 Mar 2002 | K001638 | O-RING PROSTHETIC ATTACHMENT | DZE Root-Form Endosseous Implant |
| 5 Jul 2001 | K003818 | TITANIUM ABUTMENT HEADS FOR IMZ IMPLANTS | DZE Root-Form Endosseous Implant |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| TITAN IMPLANTS, INC.FDA reg. 2249649 | BERGENFIELD, NJ, United States | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9041410). 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.