3M Deutschland GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K220257PermadyneFebruary 1, 2022
K192992Suglue 3November 5, 2019
K192961ADH19October 31, 2019
K173318Rapid HB, Rapid LB, Rapid MBOctober 31, 2017
K161922XP202September 1, 2016
K153174Ketac Universal AplicapApril 13, 2016
K151748Clean & MoreMarch 11, 2016
K151144SuPro 100September 14, 2015
K140684CLINPRO PROPHY POWDEROctober 24, 2014
K133436FLASH AR; FLASH AR QUICKMarch 7, 2014
K131404FLASH AR PENTA / FLASH AR PENTA QUICKMay 30, 2013
K120438FLASH (DIFFERENT MATERIALS)May 2, 2012