
ISO 5092:2025
ISO 5092:2025 Additive manufacturing for medical — General principles — Additive manufacturing of non-active implants
CDN $130.00
This publication was last reviewed and confirmed in 2025.
Additive manufacturing for medical — General principles — Additive manufacturing of non-active implants
Description
This document identifies factors that affect the safety and performance of surgical implants due to the fact that these implants are manufactured additively.
This document applies to non-active implants manufactured additively, including custom-made implants and patient-matched implants.
This document also applies to instrumentation for use in association with non-active surgical implants manufactured by additive manufacturing (AM).
While this document is not intended to apply to active implants, certain clauses or subclauses of this document can potentially still be used in the context of active implants.
This document identifies factors which are either unique to additively manufactured implants or which require additional consideration for additively manufactured implants. These factors have not always been included within existing implant specific standards.
This document is not applicable to implants which contain or incorporate tissues or cells, or their derivates, of animal or human origin.
Edition
1
Published Date
2026-06-19
Status
PUBLISHED
Pages
11
Format 
Secure PDF
Secure – PDF details
- Save your file locally or view it via a web viewer
- Viewing permissions are restricted exclusively to the purchaser
- Device limits - 3
- Printing – Enabled only to print (1) copy
See more about our Environmental Commitment
Abstract
This document identifies factors that affect the safety and performance of surgical implants due to the fact that these implants are manufactured additively.
This document applies to non-active implants manufactured additively, including custom-made implants and patient-matched implants.
This document also applies to instrumentation for use in association with non-active surgical implants manufactured by additive manufacturing (AM).
While this document is not intended to apply to active implants, certain clauses or subclauses of this document can potentially still be used in the context of active implants.
This document identifies factors which are either unique to additively manufactured implants or which require additional consideration for additively manufactured implants. These factors have not always been included within existing implant specific standards.
This document is not applicable to implants which contain or incorporate tissues or cells, or their derivates, of animal or human origin.
Previous Editions
Can’t find what you are looking for?
Please contact us at:
Related Documents
-

ISO 13666:2019 Ophthalmic optics – Spectacle lenses – Vocabulary
CDN $85.00 Add to cart -

ISO 16443:2014 Dentistry – Vocabulary for dental implants systems and related procedure
CDN $130.00 Add to cart -

ISO 20560:2024 Safety information for the content of piping systems and tanks – Part 1: Piping systems
CDN $259.00 Add to cart -

ISO 15223:2025 Medical devices – Symbols to be used with information to be supplied by the manufacturer – Part 1: General requirements – Amendment 1: Addition of defined term for authorized representative and modified EC REP symbol to not be country or region specific
CDN $35.00 Add to cart







