FDA Device Intelligence
HomeFKG Dentaire Sàrl › K-FILES FLEX

K-FILES FLEX

FKG Dentaire Sàrl · Model 01.554.31.008.CG · UDI-DI 07640142417613

EKS Prescription
10
510(k) clearances
3,925
Adverse events
3
Recalls
165
Facilities

Description

Flex. K-Files 554, 31 mm, # 8, handle SMG

Recalls

DateFirmReason
2025-01-02US Endodontics, LLCDue to devices being irradiated above the established specification which my result in package integrity issues.
2012-12-12Ormco/SybronendoThe length markings on the Lightspeed LSX files were wrong.
2008-08-01Ormco CorporationA recall was initiated because SybronEndo has confirmed that the K3 Engine File G-Pack has label packaging and file mis-marking error.

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.