Elipar™ DeepCure-S 76976Recalls & reported problems
3M Deutschland GmbH · 3M™ ESPE™ Elipar™ DeepCure-S LED Curing Light, 120V, NA, 76976. Sterilization prior to use only for component "Light Guide". Do not sterilize the device itself. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI J001702011438670), received between Jul 18, 2017 and Jul 18, 2017 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 18, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ON (B)(6) 2017, 3M WAS NOTIFIED THAT A (B)(6) FEMALE PATIENT REQUIRED ROOT CANAL TREATMENT ON TOOTH #28 FOLLOWING A DENTAL TREATMENT WITH 3M ESPE FILTEK BULK FILL POSTERIOR RESTORATIVE AND 3M ESPE ELIPAR DEEP CURE-S LED CURING LITE.
Patient problems: No Code Available
MAUDE report 6723564 ↗
Other ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION devices
- SmartLite® Pro Modular LED Curing Light 644400Dentsply International Inc. · ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION7 reports
- Essentials 5701741Henry Schein, Inc. · ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION1 report
- VALO 5972Ultradent Products, Inc. · ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION1 report
- Henry Schein 5703853Henry Schein, Inc. · ACTIVATOR, ULTRAVIOLET, FOR POLYMERIZATION1 report
- SPEC 3 60013941Coltene/Whaledent Inc · Activator, Ultraviolet, For Polymerization1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page