# Unisense Fertilitech A/S

- Location (FDA's records): Arrhus N, DK
- FDA decisions: 4 (2011–2014): 4 510(k) clearances
- Product codes: MQG (4)
- Predicates its devices cite: 6 (4 its own); citations of its devices by later devices: 8 (4 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
- Cook Ob/Gyn: 1 (https://510kreport.com/company/cook-ob-gyn)
- Nunc A/S: 1 (https://510kreport.com/company/nunc-a-s)

## Firms that cite its devices most
- Genea Biomedx Pty, Ltd.: 2 (https://510kreport.com/company/genea-biomedx)
- Vitrolife A/S: 2 (https://510kreport.com/company/vitrolife-a-s)

## Its most-cited devices
- K092183: Embryoscope and Embryoslide (2011), cited by 4
- K113075: Embryo Viewer Software (2011), cited by 2
- K111715: Embryoscope (2011), cited by 1
- K133712: Embryoviewer Software (2014), cited by 1

## Recent decisions
- K133712: Embryoviewer Software (Aug 8, 2014)
- K113075: Embryo Viewer Software (Dec 21, 2011)
- K111715: Embryoscope (Aug 11, 2011)
- K092183: Embryoscope and Embryoslide (Jan 11, 2011)

Source page: https://510kreport.com/company/unisense-fertilitech-a-s