FDA-recognized standard · Materials

ISO 5834-1: Implants for surgery - Ultra-high-molecular-weight polyethylene - Part 1: Powder form

Yes. FDA recognizes ISO 5834-1 Fourth edition 2019-02 as recognition 8-501, entered 2019-12-23.

Recognized editions of ISO 5834-1

FDA recognitions of ISO 5834-1, newest first (FDA database snapshot of 2026-09-01)
RecognitionEditionEnteredExtentTransition ends
8-501 ISO 5834-1 Fourth edition 2019-02 2019-12-23 Complete —

Regulations

FDA lists these classification regulations against ISO 5834-1: 21 CFR 888.3040, 21 CFR 888.3110, 21 CFR 888.3310, 21 CFR 888.3340, 21 CFR 888.3350, 21 CFR 888.3353, 21 CFR 888.3358, 21 CFR 888.3390, 21 CFR 888.3490, 21 CFR 888.3500, 21 CFR 888.3510, 21 CFR 888.3520, 21 CFR 888.3530, 21 CFR 888.3535, 21 CFR 888.3540, 21 CFR 888.3560, 21 CFR 888.3650, 21 CFR 888.3660, 21 CFR 888.3670, 21 CFR 888.3800, 21 CFR 888.3810.

Product codes that cite ISO 5834-1

54 FDA product codes cite ISO 5834-1, including HRY, HSN, HSX, HTY, HWC.

Source: FDA Recognized Consensus Standards database, snapshot of 2026-09-01. Search every recognition in the Consensus Standards Lookup, or browse all standards with a page.