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Sunmed, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K233098MYOTouch Muscle StimulatorAugust 2, 2024
K121743EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTINMarch 28, 2013
K081805CUFFALERTNovember 14, 2008
K062112SUNMED FOLEY CATHETERSJune 4, 2007
K955631ORTHOPLUG HARD BONE DESIGNFebruary 27, 1996
K955632ORTHOPLUG SOFT BONE DESIGNFebruary 27, 1996
K921263SUNLITE LARYNGOSCOPEJune 1, 1993