SILENTNITE— 510(k) K972424

Name: FDA 510(k) clearance K972424
Creator: U.S. Food and Drug Administration
Published: 1997-09-18

Substantially Equivalent

Glidewell Laboratories

FDA 510(k) clearance K972424 for SILENTNITE, Substantially Equivalent on 1997-09-18. Applicant: Glidewell Laboratories. Device class: 2.

Clearance details

Applicant: Glidewell Laboratories
Product code: Code LRK
Device class: Class 2
Regulation: 21 CFR 872.5570
Advisory panel: Dental
Date received: 1997-06-27
Decision date: 1997-09-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newport Beach, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LRK

product code LRK

Injury: 246
Malfunction: 1,044
Total: 1,290

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.