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Develops and manufactures dental implant systems with proprietary PDL® laser surface technology made of titanium.

BI

BiomateSWISS GmbH

Crissier (CH)New on Amplifa

GmbHLegal Form
Crissier, SwitzerlandHeadquarters

About BiomateSWISS

BiomateSWISS is an internationally active company for dental implant systems headquartered in Crissier, Switzerland. The company develops implant solutions at the intersection of engineering, biology, and clinical practice. The titanium implants are manufactured in Taiwan in an integrated process covering product development, precision manufacturing, laser surface treatment, prosthetic development, quality management, and traceability. At the core is the proprietary PDL® laser surface technology, which creates a defined micro- and nanostructure on the titanium surface by means of precision laser processing. The portfolio includes implants (BiomatePlus), abutments, implant motors and the Dental Unit X1, as well as the BIOnavi platform for digitally planned implant surgery with 3D imaging. The company works with distributors, clinics, and research institutions worldwide and offers technical training, professional development, and regulatory documentation.

Site
Crissier
Processes
PDL® Laser Surface Technology (laser surface treatment of titanium implants), Precision Manufacturing of Dental Implants (integrated process: design, precision manufacturing), Sterilization and Packaging (highly automated process), Quality Control per Batch according to International Standards (FDA Class II 510(k), CE), BiomatePlus Dental Fixture Design (implant design), Abutment Design (various abutment versions), BIOnavi Digital Implant Surgery (digital implant planning with 3D imaging), Digital Implant Surgery (BIOnavi, 3D Imaging / Guided Surgery)
Materials
Titanium, Laser Surface Technology
Certificates
CE Marking, FDA Class II 510(k) Clearance
Industries
Dentistry / Dental Implantology, Medical Technology
  1. 01

    Product Development (Switzerland)

  2. 02

    Implant Design (BiomatePlus Fixture, Abutments)

  3. 03

    Precision Manufacturing (Taiwan)

  4. 04

    PDL® Laser Surface Treatment

  5. 05

    Quality Control per Batch

  6. 06

    Sterilization and Packaging

  7. 07

    Regulatory Documentation and Distribution

Materials & Processes

Ti

Titanium

Material for dental implants and abutments; the PDL® laser treatment creates a defined micro- and nanotopography of the titanium surface.

PDL®

Laser Surface Technology

Precision laser processing of the titanium implant surface with defined microstructures and microchannels.

Locations

Crissier

CH

Headquarters

Industries

Dentistry / Dental ImplantologyMedical Technology

Processes & technical limits

ProcessesToleranceMax. partWeightLot sizeMaterials
PDL® Laser Surface Technology (laser surface treatment of titanium implants)Surface––––Titanium
Precision Manufacturing of Dental Implants (integrated process: design, precision manufacturing)Engineering––––Titanium
Sterilization and Packaging (highly automated process)Surface–––per batchTitanium
Quality Control per Batch according to International Standards (FDA Class II 510(k), CE)Testing–––––
BiomatePlus Dental Fixture Design (implant design)Engineering––––Titanium
Abutment Design (various abutment versions)Engineering––––Titanium
BIOnavi Digital Implant Surgery (digital implant planning with 3D imaging)Engineering–––––

2 Anlagen & Maschinen

MachineManufacturer / modelQuantityWorking areaYear builtSite
Dental Unit / Dental ChairBiomateSWISS X1––––
Implant Motor (Surgery Motor)BiomateSWISS Biomate Implant Motor––––

Additional services

Digital Implant Surgery (BIOnavi, 3D Imaging / Guided Surgery)Technical Training and Professional DevelopmentRegulatory and Technical DocumentationScientific Exchange / Research CollaborationsLaser Surface Treatment of Titanium Implants (PDL®)

Quality

Every batch undergoes quality control according to international standards. The company holds FDA Class II 510(k) Clearance and CE marking; manufacturing is carried out in highly automated processes including production, inspection, sterilization, and packaging.

EvidenceCrissier
FDA Class II 510(k) Clearance
CE Marking
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