# Vitrolife A/S

- Location (FDA's records): Viby J, DK
- FDA decisions: 4 (2015–2022): 4 510(k) clearances
- Product codes: MQK (2), PBH (1), MQG (1)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 4 (2 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
- Unisense Fertilitech A/S: 2 (https://510kreport.com/company/unisense-fertilitech-a-s)
- Auxogyn, Inc.: 1 (https://510kreport.com/company/auxogyn)

## Firms that cite its devices most
- Hua Yue Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/hua-yue-medical-technology)
- Wuhan Huchuang Union Technology Co., Ltd.: 1 (https://510kreport.com/company/wuhan-huchuang-union-technology)

## Its most-cited devices
- K173264: EmbryoScope+ (2018), cited by 3
- K150961: EmbryoSlide Culture Dish (2015), cited by 1

## Recent decisions
- K213869: EmbryoSlide+ ic8 dish (Mar 11, 2022)
- K182798: KIDScore D3 (Jul 19, 2019)
- K173264: EmbryoScope+ (May 11, 2018)
- K150961: EmbryoSlide Culture Dish (Dec 4, 2015)

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