K251205

Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants

510(k) number: K251205
Device name: Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants
Applicant: Dentsply Sirona PA · US
Product code: NHA — Abutment, Implant, Dental, Endosseous
Decision date: 2025-11-21
Date received: 2025-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Advisory committee: Dental

Also available from FDA: K251205.pdf

Official FDA record: K251205

Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.