DIGITEK TITANIUM ABUTMENT— 510(k) K141970

Name: FDA 510(k) clearance K141970
Creator: U.S. Food and Drug Administration
Published: 2015-07-31

Substantially Equivalent

Digitek Dental Solutions Limited

FDA 510(k) clearance K141970 for DIGITEK TITANIUM ABUTMENT, Substantially Equivalent on 2015-07-31. Applicant: Digitek Dental Solutions Limited. Device class: 2.

Clearance details

Applicant: Digitek Dental Solutions Limited
Product code: Code NHA
Device class: Class 2
Regulation: 21 CFR 872.3630
Advisory panel: Dental
Date received: 2014-07-21
Decision date: 2015-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kowloon, Hong Kong, CN

Download summary PDF View on FDA.gov ↗

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Adverse events under product code NHA

product code NHA

Injury: 1,270
Malfunction: 2,860
Total: 4,130

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.