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# Pelvic Organ Prolapse Mesh into Class 3
- URL: https://www.fdaweb.com/pelvic-organ-prolapse-mesh-into-class-3/
- Published: 2016-01-05T12:00:00.000Z
- Updated: 2026-09-15T02:25:10.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5134349

*Federal Register* Final order: FDA is issuing a final order to reclassify surgical mesh for transvaginal pelvic organ prolapse repair from Class 2 to Class 3, based on the determination that general controls and special controls together are not sufficient to provide reasonable assurance of safety and effectiveness for this device, and these devices present a potential unreasonable risk of illness or injury. To view this final order, click [here](https://www.gpo.gov/fdsys/pkg/FR-2016-01-05/pdf/2015-33165.pdf?ref=fdaweb.com).