# Neolight, LLC

- Location (FDA's records): Pleasanton, CA
- FDA decisions: 2 (2017–2023): 2 510(k) clearances
- Product codes: HKI (1), LBI (1)
- Predicates its devices cite: 3 (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
- Phoenix Technology Group, Inc. Dba Phoenix Clinical: 1 (https://510kreport.com/company/phoenix-technology-group-dba-phoenix-clinical)
- Natus Medical, Inc.: 1 (https://510kreport.com/company/natus-medical)
- Ohmeda Medical: 1 (https://510kreport.com/company/ohmeda-medical)

## Recent decisions
- K223575: Phoenix ICON, Phoenix ICON GO (Sep 6, 2023)
- K170585: Skylife (Oct 27, 2017)

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