IMPLANTER DENTAL PLANNING SOFTWARE— 510(k) K173083

Substantially Equivalent

Implanter, LLC

FDA 510(k) clearance K173083 for IMPLANTER DENTAL PLANNING SOFTWARE, Substantially Equivalent on 2018-12-03. Applicant: Implanter, LLC.

Clearance details

Applicant: Implanter, LLC
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2017-09-29
Decision date: 2018-12-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aventura, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.