# Silq Technologies Corporation

- Location (FDA's records): Sunny Isles Beach, FL
- FDA decisions: 3 (2022–2024): 3 510(k) clearances
- Names in FDA's records: Silq Technologies Corporation (2); Silq Technologies, Corp. (1)
- Product codes: EZL (3)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 2 (2 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
- Pathway, LLC: 1 (https://510kreport.com/company/pathway)

## Its most-cited devices
- K221625: 2-Way 100% Silicone ClearTract Catheter (2022), cited by 1
- K222118: 2-Way 100% Silicone Cleartract Catheter (2022), cited by 1

## Recent decisions
- K233013: 2-Way 100% Silicone Cleartract Catheter (Jan 23, 2024)
- K222118: 2-Way 100% Silicone Cleartract Catheter (Dec 1, 2022)
- K221625: 2-Way 100% Silicone ClearTract Catheter (Jul 1, 2022)

Source page: https://510kreport.com/company/silq-technologies