Medical Device Manufacturer · US , Alpharetta , GA

Medipurpose Pte. , Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2010
5
Total
5
Cleared
0
Denied

FDA 510(k) cleared devices by Medipurpose Pte. , Ltd. General & Plastic Surgery ✕

5 devices
1-5 of 5
Cleared Sep 22, 2022
SurgiLance® Safety Lancet
K222224 · FMK
General & Plastic Surgery · 59d
Cleared Feb 11, 2013
BABYLANCE HEEL INCISION DEVICE
K130132 · FMK
General & Plastic Surgery · 24d
Cleared Sep 01, 2011
MEDIPLUS-FOAM AG
K110062 · FRO
General & Plastic Surgery · 234d
Cleared Oct 21, 2010
SURGILANCE SAFETY LANCETS, MODELS SLN100, SLN200, SLN240, SLN300, SLB200, SLB250
K101145 · FMK
General & Plastic Surgery · 181d
Cleared Oct 19, 2010
BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200
K101417 · FMK
General & Plastic Surgery · 152d
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