LIGHTSPEED DENTAL HAND INSTRUMENT— 510(k) K932529

Substantially Equivalent

Lightspeed Endodontics

FDA 510(k) clearance K932529 for LIGHTSPEED DENTAL HAND INSTRUMENT, Substantially Equivalent on 1993-11-04. Applicant: Lightspeed Endodontics.

Clearance details

Applicant: Lightspeed Endodontics
Product code: Code EKS
Advisory panel: Dental
Date received: 1993-05-25
Decision date: 1993-11-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code EKS

product code EKS

Malfunction: 1,949
Total: 1,949

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.