# Ultrasight, Ltd.

- Location (FDA's records): Ness Ziona, IL
- FDA decisions: 3 (2023–2025): 3 510(k) clearances
- Names in FDA's records: Ultrasight , Ltd. (2); Ultrasight, Inc. (1)
- Product codes: QJU (2), QIH (1)
- Predicates its devices cite: 2 (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
- Bay Labs, Inc.: 1 (https://510kreport.com/company/bay-labs)
- Dia Imaging Analysis, Ltd.: 1 (https://510kreport.com/company/dia-imaging-analysis)

## Recent decisions
- K252235: PVAD IQ Software (Dec 18, 2025)
- K251416: UltraSight Guidance (Dec 17, 2025)
- K223347: UltraSight AI Guidance (Jul 24, 2023)

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