# Sunlight Medical, Inc.

- Location (FDA's records): Jacksonville, FL
- FDA decisions: 2 (2008–2010): 2 510(k) clearances
- Product codes: MQH (2)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (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
- Humagen Fertility Diagnostics, Inc.: 1 (https://510kreport.com/company/humagen-fertility-diagnostics)

## Recent decisions
- K092554: Blastomere Biopsy Pipettes, Polar Body Biopsy Pipettes (Apr 30, 2010)
- K072600: Intracytoplasmic Sperm and Spermatid Injection, Holding, Zone Drilling, Partial Zone Dissection and Denuding Pipettes (May 19, 2008)

Source page: https://510kreport.com/company/sunlight-medical