SILIMED NASAL L SHAPED IMPLANT— 510(k) K981833

Name: FDA 510(k) clearance K981833
Creator: U.S. Food and Drug Administration
Published: 1998-06-26

Substantially Equivalent

Silimed, LLC

FDA 510(k) clearance K981833 for SILIMED NASAL L SHAPED IMPLANT, Substantially Equivalent on 1998-06-26. Applicant: Silimed, LLC. Device class: 2.

Clearance details

Applicant: Silimed, LLC
Product code: Code FZE
Device class: Class 2
Regulation: 21 CFR 878.3680
Advisory panel: General, Plastic Surgery
Date received: 1998-05-26
Decision date: 1998-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, US

Download summary PDF View on FDA.gov ↗

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K981850 — SILIMED CHIN IMPLANTS1998-07-09
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Adverse events under product code FZE

product code FZE

Injury: 138
Total: 138

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.