Mar-Med Co.

Mar-Med Co. holds 1 FDA 510(k) medical device clearance, cleared in 1993, with 1 FDA device recall on record.

FDA recalls by Mar-Med Co.

Z-0945-2021 — Tourni-Cot - Universal, UDI 00855364004085, Model Number TCU, Non-pneumatic Tourniquet - Product Usage: The device is intended to be used in surgery on fingers or toes to provide a blood-less field.Class II·Terminated·2020-12-28

Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.

Recent clearances by Mar-Med Co.

K924223 — MAR-MED LIVER STRAPCode GDJ·1993-03-18

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

Top product codes for Mar-Med Co.

FDA recalls by Mar-Med Co.

Recent clearances by Mar-Med Co.