# Genosis, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (2003–2004): 2 510(k) clearances
- Names in FDA's records: Genosis , Ltd. (1); Genosis, Inc. (1)
- Product codes: POV (1), NGA (1)
- Predicates its devices cite: 8 (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
- Syva Co.: 1 (https://510kreport.com/company/syva)
- Embryotech Laboratories, Inc.: 1 (https://510kreport.com/company/embryotech-laboratories)
- Hamilton Thorne Research: 1 (https://510kreport.com/company/hamilton-thorne-research)
- Humagen Fertility Diagnostics, Inc.: 1 (https://510kreport.com/company/humagen-fertility-diagnostics)
- Genua 1944, Inc.: 1 (https://510kreport.com/company/genua-1944)
- Abbott Laboratories: 1 (https://510kreport.com/company/abbott-laboratories)
- Serono Diagnostics, Inc.: 1 (https://510kreport.com/company/serono-diagnostics)
- Armkel, LLC: 1 (https://510kreport.com/company/armkel)

## Firms that cite its devices most
- Princeton BioMeditech Corp.: 2 (https://510kreport.com/company/princeton-biomeditech)
- Motilitycount Aps: 1 (https://510kreport.com/company/motilitycount)
- Quantrx Biomedical Corporation: 1 (https://510kreport.com/company/quantrx-biomedical)

## Its most-cited devices
- K041039: Fertell Male Fertility Test (2004), cited by 3
- K032002: Fertell Female Fertility Test (2003), cited by 1

## Recent decisions
- K041039: Fertell Male Fertility Test (Jul 20, 2004)
- K032002: Fertell Female Fertility Test (Oct 30, 2003)

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