Merit Medical Ireland, Ltd.

Merit Medical Ireland, Ltd. holds 6 FDA 510(k) medical device clearances, first cleared 2012, most recent 2026.

Name variants for Merit Medical Ireland, Ltd.

as filed with FDA

Merit Medical Ireland, Ltd.5 devices
Merit Medical Ireland , Ltd.1 device

Top product codes for Merit Medical Ireland, Ltd.

DQX — Cardiovascular5 devices
MAV — Cardiovascular1 device

Recent clearances by Merit Medical Ireland, Ltd.

K261640 — Merit MAK Nitinol/Gold-Tungsten Guide WireCode DQX·2026-07-13
K254137 — InQwire Amplatz Guide WireCode DQX·2026-05-22
K253847 — Splashwire Hydrophilic Guide Wire (MSWSTD35150J3)Code DQX·2026-01-31
K251385 — InQwire Super Stiff Guide Wire (6 models)Code DQX·2026-01-21
K251181 — Splashwire Hydrophilic Guide Wire (6 models)Code DQX·2025-08-29
K122321 — BASIXCONPAK ANALOG INFLATION SYRINGECode MAV·2012-12-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.