IMPROVIS IMAGING SYSTEM— 510(k) K101654

Substantially Equivalent

American Dental Partners, Inc.

FDA 510(k) clearance K101654 for IMPROVIS IMAGING SYSTEM, Substantially Equivalent on 2010-11-10. Applicant: American Dental Partners, Inc..

Clearance details

Applicant: American Dental Partners, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2010-06-11
Decision date: 2010-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wakefield, MA, US

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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.