# Dxnow, Inc.

- Location (FDA's records): Gaithersburg, MD
- FDA decisions: 1 (2018–2018): 1 510(k) clearance
- Product codes: MQK (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (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
- Menicon Co., Ltd. New Business Division: 1 (https://510kreport.com/company/menicon-co-new-business-division)

## Firms that cite its devices most
- Motilitycount Aps: 1 (https://510kreport.com/company/motilitycount)
- Ipreg Incorporation: 1 (https://510kreport.com/company/ipreg-incorporation)
- Cytoswim, Ltd.: 1 (https://510kreport.com/company/cytoswim)
- Bonraybio Co., Ltd.: 1 (https://510kreport.com/company/bonraybio)

## Its most-cited devices
- K173075: ZyMot ICSI Sperm Separation Device, ZyMot Multi Sperm Separation Device (850µl, 3ml) (2018), cited by 4

## Recent decisions
- K173075: ZyMot ICSI Sperm Separation Device, ZyMot Multi Sperm Separation Device (850µl, 3ml) (Mar 8, 2018)

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