Indications for use
The clinical indications and intended patient population the implant series is designed and validated for.
i-Fix Instructions for Use
Every IFU,
one place.
Instructions for Use for every current i-Fix series — indications, contraindications and intended use, straight from the source document.
02 What's inside an IFU
Four things every
IFU documents.
Contraindications & warnings
Conditions, comorbidities and use cases the manufacturer specifically advises against or flags as a risk factor.
Handling & sterility
Packaging integrity, single-use status and handling instructions before an implant reaches the surgical tray.
Material & traceability
Alloy grade, surface designation and the lot/batch traceability information printed on the IFU and the package label.
03 Download
Instructions for Use,
by series.
Instructions for Use IP Series IP-Series.pdf Download PDF ↗ Instructions for Use SP Series SP-Series.pdf Download PDF ↗ Instructions for Use AK Series Apex Konnect.pdf Download PDF ↗ Instructions for Use ZE Series ZE-Series.pdf Download PDF ↗ Instructions for Use C Series C-Series.pdf Download PDF ↗ Instructions for Use B Series B-Series.pdf Download PDF ↗
Not yet published here: IP+ Series, AK* Series, PSI Series, Crown Series — request the current document through Contact.
Drafted with the productNot a separate afterthought
04 Regulatory documentation
The same content
printed on the package insert.
An IFU is drafted alongside the packaging and label, not written up separately afterward — the indications and handling instructions inside it are what's on the physical package that ships.
05 Frequently asked
Before you
download.
The manufacturer document covering indications, contraindications, warnings and the intended surgical or prosthetic use of a dental implant series — required reading before a device is used clinically.
Every series with a published IFU is listed on this page as a direct PDF. Series without one listed yet are available on request through Contact.
Each card shows the revision, issue date and document number printed on the PDF itself. Request the latest verified revision directly if anything is time-sensitive for a live case.
Catalogs sit alongside these IFUs in the Digital Library and Downloads page, and per-series inside each product's own Documents tab.
No. The IFU documents the manufacturer's intended use, warnings and handling — treatment planning and patient selection remain the responsibility of the qualified clinician.
Not sure what a term in the IFU means? See the glossary →
Need an IFU that isn't listed here?
Request the current revision directly — the team keeps the full document set on file.