# K232677: Reia pessary

- Pathway: 510(k) (Traditional)
- Applicant: Reia, LLC
- Decided: May 21, 2024 after 263 days
- Product code: HHW (Pessary, Vaginal)
- Device class: 2
- Regulation: 21 CFR 884.3575
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K092981 (2010). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K190277: ProVate Vaginal Support, Contipi Medical, Ltd. (2019) Summary page 5.

## Indications for use
The Reia pessary is indicated for the temporary, non-surgical management of Pelvic Organ Prolapse.

Source page: https://510kreport.com/device/K232677
Methodology: https://510kreport.com/methodology