Swiss manufacturing tolerances,
documented international use
NTA Implant is a brand of Pilatus Swiss Dental GmbH, Switzerland.
NTA manufactures dental implants and prosthetic components for implantology. Product development, manufacturing, marketing, and trademark rights are held by the company. Fixture geometry and surface processing follow current implantology literature and specified manufacturing methods.
CORPORATE
Screw-retained and press-fit systems
The portfolio includes both screw-retained and press-fit implant systems, with matching prosthetic accessories.
NTA IMPLANT
Under the NTA Implant, NTA Spure, NTA Shorter, NTA Shorter Plus, and NTA Hybrid marks, screw-retained and press-fit fixtures are manufactured, together with the matching prosthetic accessories.
Quality-management certificates held by the company:
FDA, CE, MDR, ISO 9001:2015, ISO 13485:2016, ISO 10002:2018.
Partners in the United States, Switzerland, South Korea, and France carry out R&D, manufacturing, and surface processing in those countries. Some partners have more than 35 years of activity in the dental market.
Vision & mission
Mission: supply a product range covering documented dental-implant indications, without reducing specified manufacturing controls, so that placement and restorative protocols in the IFU can be followed.
Vision: develop a multi-system implant portfolio informed by current research and manufacturing methods, combining specified quality controls, design updates, and accessible pricing for the markets served.
Need-specific components are produced with current manufacturing methods and supplied through documented distribution channels. Placement must follow the IFU for the fixture and abutment selected.
SLA surface science
Fixtures are developed against current implantology data, using documented methods such as SLA grit-blast and acid-etch to support bone–implant contact (BIC).
Regulatory standards
FDA, CE, ISO 9001, and ISO 13485 apply to quality-system and sterilization controls in the markets where those certificates are in force. Production is MDR-aligned.
Clinical support
Supply includes surgical kits, digital libraries, and training — not the fixture alone — so the osteotomy and restorative workflow can be followed per IFU.
