# Artiglass Srl

- Location (FDA's records): Due Carrare, IT
- FDA decisions: 2 (2013–2022): 2 510(k) clearances
- Product codes: QEH (1), FMF (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 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
- Spectra Medical Devices, Inc.: 1 (https://510kreport.com/company/spectra-medical-devices)

## Its most-cited devices
- K122416: Artiglass L. O.R. Glass Syringe (2013), cited by 1

## Recent decisions
- K213800: Artiglass NRFitTM Tip L.O.R. Glass Syringes (May 19, 2022)
- K122416: Artiglass L. O.R. Glass Syringe (May 3, 2013)

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