Medipurpose Pte. , Ltd.

Medipurpose Pte. , Ltd. holds 5 FDA 510(k) medical device clearances, first cleared 2010, most recent 2022.

Top product codes for Medipurpose Pte. , Ltd.

FMK — General, Plastic Surgery4 devices
FRO — Unknown1 device

Recent clearances by Medipurpose Pte. , Ltd.

K222224 — SurgiLance® Safety LancetCode FMK·2022-09-22
K130132 — BABYLANCE HEEL INCISION DEVICECode FMK·2013-02-11
K110062 — MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AGCode FRO·2011-09-01
K101145 — SURGILANCE SAFETY LANCETS, MODELS SLN100, SLN200, SLN240, SLN300, SLB200, SLB250Code FMK·2010-10-21
K101417 — BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200Code FMK·2010-10-19

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