FDA Device Intelligence
HomeDENTMATE TECHNOLOGY CO., LTD. › LEDEX

LEDEX

DENTMATE TECHNOLOGY CO., LTD. · Model WL-070 · UDI-DI 04719873920105

EBZ Prescription
1
510(k) clearances
171
Adverse events
4
Recalls
103
Facilities

Description

WL-070 Orange (US)

Recalls

DateFirmReason
2022-01-20Envisiontec US LlcThe PCA 4000 may not fully cure EnvisionTEC dental resins to desired product specifications.
2018-04-04Handpiece HeadquartersTip of the curing light was too hot causing a heat sensation in the patients.
2014-04-14Ivoclar Vivadent, Inc.A stock check revealed broken glass fibers between the connector and the fiber bundle in a large number of these light probes.
2012-04-23O'Ryan Industries IncDisposa-Shield Disposable Curing Shield is recalled due to lacking 510K, PMA or IDE, and inadequate quality system.

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.