Arca
Skip to content

3M ESPE Dental Products

Medical device makerAI in GermanyAI, part of 3MAI. FDA records under 3 spellings of its name, each linked to the record.

  • 510(k) clearances: 37

Records by Year

Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date

Latest Records

Newest first across sources; each opens the record
DateRecordSource
May 10, 20233M™ Clinpro™ Clear 2.1% Sodium Fluoride TreatmentK231338 · LBH510(k) clearances
Feb 6, 20233M™ VitCal Liner/BaseK230270 · EJK510(k) clearances
Jun 13, 20223M Filtek Supreme Flowable RestorativeK221695 · EBF510(k) clearances
May 29, 20193M RelyX Pediatric Resin Modified Glass Ionomer CementK191122 · EMA510(k) clearances
Jan 2, 20193M Filtek Universal RestorativeK183476 · EBF510(k) clearances
May 8, 2014FILTEK BULK FILL POSTERIOR RESTROATIVEK141081 · EBF510(k) clearances
Mar 19, 2012FILTEK BULK FILL FLOWABLE RESTORATIVEK120453 · EBF510(k) clearances
May 5, 2011RELYX LUTING PLUS AUTOMIXK111185 · EMA510(k) clearances

Canada and Imports

Matched by company name
Active Health Canada device licences
25, as of Nov 10, 2026
FDA import refusals since 2024
51 shipment lines, through Oct 23, 2026

Names and Identifiers

Appears as
3M Espe AG Dental Products3M Espe Dental Products3M Company Espe Dental Products

Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built

Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.