# Fertiligent, Ltd.

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 2 (2010–2015): 2 510(k) clearances
- Product codes: MQF (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Catheter Research, Inc.: 1 (https://510kreport.com/company/catheter-research)

## Firms that cite its devices most
- Catheter Research, Inc.: 1 (https://510kreport.com/company/catheter-research)

## Its most-cited devices
- K092579: Intrauterine Insemination (Iui) Catheter (2010), cited by 2

## Recent decisions
- K141666: Fertiligent Slow Release Iui Catheter Kit (Feb 3, 2015)
- K092579: Intrauterine Insemination (Iui) Catheter (Apr 2, 2010)

Source page: https://510kreport.com/company/fertiligent