APX21— 510(k) K073185

Substantially Equivalent

Techdent Technologies, Ltd.

FDA 510(k) clearance K073185 for APX21, Substantially Equivalent on 2008-03-06. Applicant: Techdent Technologies, Ltd..

Clearance details

Applicant: Techdent Technologies, Ltd.
Product code: Code LQY
Advisory panel: Unknown
Date received: 2007-11-13
Decision date: 2008-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: M.P. Misgav, IL

Download summary PDF View on FDA.gov ↗

Adverse events under product code LQY

product code LQY

Malfunction: 504
Total: 504

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.