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.
6Series covered
PDFDirect download
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.
04 Reading a revision
Before you rely
on a document.
Check the revision or issue date printed on the document itself against what's linked here — the file here is refreshed when the manufacturer issues a new one, but the source document is always the authoritative reference for a live case. If a revision date is missing or looks out of date, request the current file directly rather than relying on a cached copy.
Drafted with the productNot a separate afterthought
05 Written for the packaging line, not marketing
The same warnings
printed on the box.
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.
06 Frequently asked
Before you
download.
What is an IFU?
Instructions for Use — the manufacturer document covering indications, contraindications, warnings and the intended surgical/prosthetic use of an implant series.
Is every series listed here?
Every series with a published IFU in the current document set. Series without one listed above are available on request through Contact.
Are these the current revisions?
Each card shows the revision, issue date and document number printed on the PDF itself (all current IFUs are Rev-01, IFU-03-050320, dated 05 Mar 2020). Request the latest verified revision for anything time-sensitive.
Where do product catalogs live?
Catalogs sit alongside these IFUs in the Digital Library, and per-series in each product's Documents tab.
Does the IFU replace clinical judgement?
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.