LightForce Orthodontic System (LFO System)— 510(k) K200148

Name: FDA 510(k) clearance K200148
Creator: U.S. Food and Drug Administration
Published: 2020-02-21

Substantially Equivalent

Lightforce Orthodontics

FDA 510(k) clearance K200148 for LightForce Orthodontic System (LFO System), Substantially Equivalent on 2020-02-21. Applicant: Lightforce Orthodontics. Device class: 2.

Clearance details

Applicant: Lightforce Orthodontics
Product code: Code NJM
Device class: Class 2
Regulation: 21 CFR 872.5470
Advisory panel: Dental
Date received: 2020-01-22
Decision date: 2020-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cambridge, MA, US

Download summary PDF View on FDA.gov ↗

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