# K993953: Oves Cervical Cap

- Pathway: 510(k) (Traditional)
- Applicant: Veos, Ltd.
- Decided: Mar 21, 2000 after 120 days
- Product code: HDR (Cap, Cervical)
- Device class: 2
- Regulation: 21 CFR 884.5250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 2 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K063227: Conceivex Conception Kit (2007), 3 descendants of its own
- K222969: FERTI-LILY Conception Cup (2023), 1 descendant of its own
- K112200: Focus Touch Conception System (2012), 1 descendant of its own
- K242031: Béa Applicator  (BAP-GB-01) (2025), 0 descendants of its own
- K140186: The Stork Otc (2014), 0 descendants of its own

## Indications for use
The Oves Cervical Cap is indicated for use in artificial insemination procedures in situations in which low sperm count, sperm immotility, or hostile vaginal environment have been diagnosed. The Oves Cervical Cap removes semen from the vaginal environment and concentrates the sperm at the opening of the cervical os, thus facilitating sperm contact with cervical mucosa.

Source page: https://510kreport.com/device/K993953
Methodology: https://510kreport.com/methodology