Palliare , Ltd. is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Palliare , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: EVA15 insufflator, EVA5 Insufflator, EVA15 insufflator
6
Total
6
Cleared
0
Denied
Palliare , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Galway, IE.
Latest FDA clearance: May 2024. Active since 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Palliare , Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Palliare Ltd. C/O Promedic Consulting, LLC, Palliare, Ltd. C/O Promedic, LLC and ProMedic Consulting, LLC.
FDA 510(k) Regulatory Record - Palliare , Ltd.
6 devices
Cleared
May 02, 2024
EVA15 insufflator
Obstetrics & Gynecology
227d
Cleared
Mar 24, 2023
EVA5 Insufflator
Gastroenterology & Urology
30d
Cleared
Jan 27, 2023
EVA15 insufflator
Obstetrics & Gynecology
126d
Cleared
Jul 08, 2021
END 200 Endoscopic Tubeset
Gastroenterology & Urology
282d
Cleared
Oct 21, 2020
EVA15
Obstetrics & Gynecology
28d
Cleared
Jul 23, 2020
EVA 15 Insufflator
Obstetrics & Gynecology
217d