# Palliare, Ltd.

- Location (FDA's records): Galway, IE
- FDA decisions: 6 (2020–2024): 6 510(k) clearances
- Product codes: HIF (4), FCX (2)
- 510(k) review time since 2016: median 172 days, against 99 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 7 (5 its own); citations of its devices by later devices: 6 (5 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
- E-Z-Em, Inc.: 1 (https://510kreport.com/company/e-z-em)
- Conmed Corporation: 1 (https://510kreport.com/company/conmed)

## Firms that cite its devices most
- Vision Medical, Inc.: 1 (https://510kreport.com/company/vision-medical)

## Its most-cited devices
- K222901: EVA15 insufflator (2023), cited by 2
- K193520: EVA 15 Insufflator (2020), cited by 2
- K230474: EVA5 Insufflator (2023), cited by 1
- K202799: EVA15 (2020), cited by 1

## Recent decisions
- K232902: EVA15 insufflator (May 2, 2024)
- K230474: EVA5 Insufflator (Mar 24, 2023)
- K222901: EVA15 insufflator (Jan 27, 2023)
- K202922: END 200 Endoscopic Tubeset (Jul 8, 2021)
- K202799: EVA15 (Oct 21, 2020)
- K193520: EVA 15 Insufflator (Jul 23, 2020)

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