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3M™ ESPE™ Impregum™ Penta™

3M Deutschland GmbH · Model P31739 · UDI-DI 04054596735705

EFDEIDELWEBH Prescription
10
510(k) clearances
6
Adverse events
1
Recalls
32
Facilities

Description

3M™ ESPE™ Impregum™ Penta™ Soft Heavy Body Polyether Impression Material Intro Kit, P31739

Recalls

DateFirmReason
2026-07-20SDI LimitedPotential for electrical discharge from unit when unplugged.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.