Clean.
Confidence at the surface.

Independent recognition. Documented quality.

Discover the evidence behind T6 Torq, from CleanImplant surface recognition to quality management and product traceability.

Discover the surface quality

Surface cleanlinessCleanImplant recognition Quality managementEU MDR & ISO documents Product identificationReferences, lots & traceability

A clean surface.
Independently recognised.

T6 Torq is recognised by CleanImplant for implant surface cleanliness.

Move from the thread profile to the finer texture of the surface, using original views from the same T6 Torq specimen series.

Independent surface assessmentExplore T6 Torq’s surface assessment

Microscopy: mmri.berlin, via CleanImplant

If the interactive explorer is unavailable, open the original microscopy images below.

The thread, in detail.

Follow the thread crest, flank and valley in this scanning electron microscope view.

T6 Torq implant surface at 500 times magnification, with the original scale bar and laboratory credit

A closer view of the surface.

Explore the texture across a wider area of the T6 Torq implant surface.

T6 Torq implant surface at 2500 times magnification, with the original scale bar and laboratory credit

The surface at another scale.

Higher magnification brings the smaller features of the surface topography into view.

T6 Torq implant surface at 5000 times magnification, with the original scale bar and laboratory credit

Finer detail. A different perspective.

Look more closely at the surface features in the highest-magnification view in this series.

Scanning electron micrograph of the complete T6 Torq implant, with the original 3 mm scale and laboratory credit

The complete implant, in perspective.

A whole-implant SEM view connects the overall thread geometry to the surface detail.

Quality, documented.
Across the T6 system.

NucleOSS’s EU MDR quality-management certificate covers the listed T6 and T6 Torq implant systems, restorative components, surgical instruments and sets.

EU MDRRegulation (EU) 2017/745

Manufacturer quality management

Quality-management certification for the named T6 and T6 Torq product groups, with the covered products identified in the original document.

View EU MDR certificate PDF

Products and documentation covered

Certificate 2975-MED-2529701 covers quality-management requirements under Annex IX, Chapters I and III of Regulation (EU) 2017/745. It was issued on 24 October 2025, with a validity date of 23 October 2030. Its conditions explain the additional technical-documentation assessments for the relevant device classes.

ISO 13485EN ISO 13485:2016

Medical-device quality management

Quality management behind NucleOSS dental-implant, abutment and surgical-instrument design, production and distribution.

View ISO 13485 certificate PDF

Manufacturer certificate details

Certificate 32104701 was issued by SZUTEST Uygunluk Değerlendirme A.Ş. to Şanlılar Tıbbi Cihazlar Medikal Kimya San. ve Tic. Ltd. Şti., the NucleOSS manufacturer. It identifies EN ISO 13485:2016 and covers design and development, production, distribution, sales and marketing of dental implants, abutments and surgical instruments.

Clarity on the label.
Detail in the record.

Keep each implant connected to its product record. Product identification makes the reference, production lot and dimensions available when you need them.

Read the product-label guide

NucleOSS manufacturer product cartons with colour-coded identification labels

REF: The exact product reference
LOT: The production lot for traceability
UDI: The unique device identification
Size & expiry: Implant dimensions and use-by information

Bring the evidenceinto your evaluation.

Discuss the implant, restorative components and instruments you are considering, with their original documentation close at hand.

Discuss your practice

Clean.Confidence at the surface.

A clean surface.Independently recognised.