FDA Device Intelligence
Home3M Deutschland GmbH › 3M™ Imprint™

3M™ Imprint™

3M Deutschland GmbH · Model 71498 · UDI-DI 04054596648296

EIDELW Prescription
10
510(k) clearances
9
Adverse events
1
Recalls
173
Facilities

Description

3M™ Imprint™ 4 Penta™ Super Quick Heavy VPS Impression Material Trial Kit, 71498

Recalls

DateFirmReason
2016-12-14Ultradent Products, Inc.Ultradent Products, Inc. announces a voluntary field action for the NanoTips 30g 20pk, 100pk because the cannula attached to the tip hub may become loose or detach from the blue ba

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.