Atlantis Abutments in Titanium
by Dentsply Sirona 510(k)
Active
510(k) K252343
Overview
The Atlantis Abutment in Titanium is a patient-specific dental device designed for use with an endosseous implant. It serves to support a cement-retained crown or bridge restoration.
This device is authorized under FDA 510K clearance. It is intended for use in dental clinical settings to facilitate prosthetic rehabilitation.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK252343 | Date9 Dec 2025 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- NHA
- Device Class
- Class II
- Regulation
- 21 CFR Part 872.3630
- Advisory Committee
- Dental
- FDA Decision
- SESE Substantially Equivalent
Other devices from Dentsply Sirona Inc
Questions
What is the primary function of the Atlantis Abutment in Titanium?
This device is a patient-specific component designed for use with an endosseous implant. Its primary purpose is to provide the necessary support for cement-retained crown or bridge dental restorations.
In what clinical environment is this device intended to be used?
The Atlantis Abutment in Titanium is intended for use specifically within dental clinical settings to facilitate the prosthetic rehabilitation of patients.
What is the regulatory status of this dental device?
The Atlantis Abutment in Titanium is authorized under FDA 510K clearance, which indicates that the device has been determined to be substantially equivalent to legally marketed predicate devices.