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Surface

SLActive®: the hydrophilic version of SLA

The same roughness as SLA, kept chemically active

SLActive® is an implant surface. FDA filings describe Straumann implants as large-grit sandblasted and acid-etched, and SLActive as being 'in a chemically activated state, which is preserved by storage in a saline solution (NaCl)'.1

Microscopic implant surface visualisation
In short
  • SLActive = the SLA roughness, kept hydrophilic (water-loving) by storage in saline.1
  • Straumann links it to faster osseointegration and immediate loading.2
  • Manufacturer survival claims are labelled as such below.

SLActive vs SLA in plain words

Both start from the same roughened titanium surface. SLA is dried and packed normally. SLActive is kept chemically clean and wet in saline, which makes it hydrophilic: water and blood spread across it instead of beading up.1 The idea is to support early bone healing.

Claims and evidence

Manufacturer claim Manufacturer documentation

Straumann states that its SLActive® surface demonstrated 100% implant survival, even in patients compromised by smoking, diabetes or radiation therapy. 3

This is how the manufacturer summarises studies it cites. A figure from selected study groups does not mean every implant will survive in every patient. We have not independently reviewed each cited study.

Systematic review

A systematic review of laboratory studies found that hydrophilic SLActive surfaces shifted immune cells towards a less inflammatory response than standard SLA surfaces. 4

These were in-vitro studies of low-to-moderate quality. The authors state they do not replicate healing in the human body.

Straumann's own website lists supporting studies; independent confirmation of manufacturer statements varies by claim. We label them rather than repeat them as fact.

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Clinical review pending. Facts on this page are checked against the sources listed below (regulatory records, manufacturer documents, peer-reviewed research). A named clinician will review it before we call it medically reviewed.
Last updated 28 Sep 2026 · How we review

Sources

  1. Regulatory recordFDA 510(k) K230108 — Straumann BLC and TLC Implants (510(k) summary) — U.S. Food and Drug Administration, 2023-09-14. Accessed 28 Sep 2026.
  2. Manufacturer documentationDental implant materials and surfaces — Institut Straumann AG. Accessed 28 Sep 2026.
  3. Manufacturer documentationStraumann iEXCEL™ system (product page) — Institut Straumann AG. Accessed 28 Sep 2026.
  4. Systematic reviewDonohoe E et al. Macrophage inflammatory response to hydrophobic vs hydrophilic SLA titanium: systematic review — Clin Exp Dent Res, 2023. Accessed 28 Sep 2026.

Educational information only. The choice of implant system depends on your anatomy, restorative plan, bone quality and the clinician's assessment. This website does not recommend a specific implant for you.

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