# Vitrolife AB

- Location (FDA's records): Washington, DC
- FDA decisions: 5 (2003–2020): 5 510(k) clearances
- Names in FDA's records: Vitrolife AB (3); Vitrolife GmbH (1); Vitrolife, Inc. (1)
- Product codes: MQL (3), MSB (1), MRX (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 6 (0 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
- Irvine Scientific Sales Co., Inc.: 3 (https://510kreport.com/company/irvine-scientific-sales)
- Vitrolife Sweden AB: 1 (https://510kreport.com/company/vitrolife-sweden)
- Research Instruments, Ltd.: 1 (https://510kreport.com/company/research-instruments)

## Firms that cite its devices most
- Vitrolife Sweden AB: 2 (https://510kreport.com/company/vitrolife-sweden)
- Sage In-Vitro Fertilization, Inc.: 2 (https://510kreport.com/company/sage-in-vitro-fertilization)
- Genea Biomedx Pty, Ltd.: 1 (https://510kreport.com/company/genea-biomedx)
- Shenzhen Vitavitro Biotech Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-vitavitro-biotech)

## Its most-cited devices
- K133568: G-TL (2014), cited by 3
- K032154: G-Freezekit Blast (2004), cited by 1
- K022730: Perfadex Solution for Lung Preservation (2003), cited by 1
- K032155: G-Thawkit Blast (2004), cited by 1

## Recent decisions
- K192008: LaserShot M, NaviLase (Mar 25, 2020)
- K133568: G-TL (Jul 16, 2014)
- K032154: G-Freezekit Blast (May 7, 2004)
- K032155: G-Thawkit Blast (May 7, 2004)
- K022730: Perfadex Solution for Lung Preservation (Oct 27, 2003)

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