# Smartlight, Ltd.

- Location (FDA's records): Nesher, IL
- FDA decisions: 2 (1997–1999): 2 510(k) clearances
- Names in FDA's records: Smartlight, Ltd. (1); Smartlight, Inc. (1)
- Product codes: IXC (2)
- 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
- Adp, Ltd.: 2 (https://510kreport.com/company/adp)
- American Medical Sales, Inc.: 1 (https://510kreport.com/company/american-medical-sales)

## Recent decisions
- K991302: Smartlight Digital Film Viewer, Models SL 4000PLUS, SL 2000PLUS (Jun 1, 1999)
- K973965: Smart Motorized Viewer (Dec 12, 1997)

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