Medipurpose Pte. , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Medipurpose Pte. , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Last cleared in 2022. Active since 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medipurpose Pte. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medipurpose Pte. , Ltd.
5 devices
Cleared
Sep 22, 2022
SurgiLance® Safety Lancet
General & Plastic Surgery
59d
Cleared
Feb 11, 2013
BABYLANCE HEEL INCISION DEVICE
General & Plastic Surgery
24d
Cleared
Sep 01, 2011
MEDIPLUS-FOAM AG
General & Plastic Surgery
234d
Cleared
Oct 21, 2010
SURGILANCE SAFETY LANCETS, MODELS SLN100, SLN200, SLN240, SLN300, SLB200, SLB250
General & Plastic Surgery
181d
Cleared
Oct 19, 2010
BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200
General & Plastic Surgery
152d