ToothWave— 510(k) DEN190039

Unknown

Home Skinovations , Ltd.

FDA 510(k) clearance DEN190039 for ToothWave, Unknown on 2020-09-17. Applicant: Home Skinovations , Ltd.. Device class: 2.

Clearance details

Applicant: Home Skinovations , Ltd.
Product code: Code QMJ
Device class: Class 2
Regulation: 21 CFR 872.6866
Advisory panel: Dental
Date received: 2019-08-22
Decision date: 2020-09-17
Decision: Unknown
Clearance type: Direct
Location: Yokneam, IL

View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.