3M Deutschland GmbH
KAMEN North Rhine-Westphalia, DE
3M Deutschland GmbH appears in FDA device records in KAMEN North Rhine-Westphalia, DE. FDA records list 12 510(k) clearances between and , no PMA records and 3 registered establishments. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 12 510(k) clearances for 3M Deutschland GmbH between 2012 and 2022. The busiest year on record is 2016, with 3. The most recent is 2022, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2012 | 1 |
| 2013 | 1 |
| 2014 | 2 |
| 2015 | 1 |
| 2016 | 3 |
| 2017 | 1 |
| 2019 | 2 |
| 2022 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K220257 | Permadyne | ELW | Substantially Equivalent | |
| K192992 | Suglue 3 | EMA | Substantially Equivalent | |
| K192961 | ADH19 | KLE | Substantially Equivalent | |
| K173318 | Rapid HB, Rapid LB, Rapid MB | ELW | Substantially Equivalent | |
| K161922 | XP202 | EIH | Substantially Equivalent | |
| K153174 | Ketac Universal Aplicap | EMA | Substantially Equivalent | |
| K151748 | Clean & More | PIP | Substantially Equivalent | |
| K151144 | SuPro 100 | EBG | Substantially Equivalent | |
| K140684 | CLINPRO PROPHY POWDER | PIP | Substantially Equivalent | |
| K133436 | FLASH AR; FLASH AR QUICK | ELW | Substantially Equivalent | |
| K131404 | FLASH AR PENTA / FLASH AR PENTA QUICK | ELW | Substantially Equivalent | |
| K120438 | FLASH (DIFFERENT MATERIALS) | ELW | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3004083376 | 3004083376 | 3M DEUTSCHLAND GMBH | Plant Kamen, KAMEN North Rhine-Westphalia 59174 DE | 2026 | |
| 3008512935 | 3008512935 | 3M Deutschland GmbH | Carl-Schurz-Str.1, Neuss North Rhine-Westphalia 41453 DE | 2026 | |
| 3015232464 | 3015232464 | 3M Deutschland GmbH | Neusser Strasse 201, Juechen North Rhine-Westphalia 41363 DE | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain