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.
6 Instructions for Use as the source PDF, covering 6 of the 10 series in the portfolio. Each card shows the revision, issue date and document number printed on the file.
02 Before clinical use
IFU contents.
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
Downloads.
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: AK* Series, IP+ Series, PSI Series, Crown Series — request the current document through Contact.
Current revisionRev-01 · IFU-03-050320
04 Regulatory documentation
In the box.
Lot, batch and reference fields in the insert match the label on the sterile pack, so a document on this page can be tied back to the pack it came out of.
05 Frequently asked
Frequently asked questions.
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.
On the Downloads page, and per-series inside each product's own Documents tab. The Digital Library is separate — it holds the exocad CAD implant libraries.
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?
Superseded revisions are held on file as well — name the series and the document number printed on the copy you have.