Manufacturer registered with FDA
American Dental Implant Corporation
New Castle, PA, United States. Lists 3 dental device types with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.
- Device types listed
- 3
- Brands and models
- 4
- 510(k) clearances
- 22004–2008
- Markets registered in
- 1United States
- Establishments
- 1United States
510(k) clearances per year, 2000–2026
Devices listed with FDA
What American Dental Implant Corporation 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 | ADI Bone DrillAmerican Dental Implant | 2007 |
| Endosseous Dental Implant AccessoriesNDP · Class 1 | Implant instruments & surgical kits | Maker | Dental Accessories for American Dental Implant System | 2018 |
| Endosseous Dental Implant AbutmentNHA · Class 2 | Implant abutments | Maker | ADI Abutment | 2008 |
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
American Dental Implant Corporation 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: Osteo Implant Corp. (2).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 14 Jul 1995 | K945706 | BONE DRILL | Osteo Implant Corp. | DZE Root-Form Endosseous Implant |
| 10 Feb 1987 | K862854 | OSTEO TITANIUM DENTAL IMPLANT | Osteo Implant Corp. | DZE Root-Form Endosseous Implant |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| AMERICAN DENTAL IMPLANT CORPORATIONFDA reg. 2523430 | New Castle, PA, United States | Repacker / relabeler, Specification developer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9061617). 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.