ELLIPSE FLEX PPT, MODEL 9ESF7255— 510(k) K052688

Substantially Equivalent

Danish Dermatologic Development A/S

FDA 510(k) clearance K052688 for ELLIPSE FLEX PPT, MODEL 9ESF7255, Substantially Equivalent on 2005-12-12. Applicant: Danish Dermatologic Development A/S.

Clearance details

Applicant: Danish Dermatologic Development A/S
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2005-09-28
Decision date: 2005-12-12
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Hoersholm, DK

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Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.