3M Deutschland GmbH

3M Deutschland GmbH holds 12 FDA 510(k) medical device clearances, first cleared 2012, most recent 2022.

Top product codes for 3M Deutschland GmbH

ELW — Dental5 devices
EMA — Dental2 devices
PIP — Dental2 devices
EBG — Dental1 device
EIH — Dental1 device
KLE — Dental1 device

Recent clearances by 3M Deutschland GmbH

K220257 — PermadyneCode ELW·2022-02-01
K192992 — Suglue 3Code EMA·2019-11-05
K192961 — ADH19Code KLE·2019-10-31
K173318 — Rapid HB, Rapid LB, Rapid MBCode ELW·2017-10-31
K161922 — XP202Code EIH·2016-09-01
K153174 — Ketac Universal AplicapCode EMA·2016-04-13
K151748 — Clean & MoreCode PIP·2016-03-11
K151144 — SuPro 100Code EBG·2015-09-14
K140684 — CLINPRO PROPHY POWDERCode PIP·2014-10-24
K133436 — FLASH AR; FLASH AR QUICKCode ELW·2014-03-07
K131404 — FLASH AR PENTA / FLASH AR PENTA QUICKCode ELW·2013-05-30
K120438 — FLASH (DIFFERENT MATERIALS)Code ELW·2012-05-02

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