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FDA 510(k), K200148, LightForce Orthodontic System (LFO System)
FDA 510(k), K200148, LightForce Orthodontic System (LFO System)
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$149.00 USD
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510(K) Number: K200148
Device Name: LightForce Orthodontic System (LFO System)
Manufacturer: LightForce Orthodontics
Device Classification Name: Bracket, Ceramic, Orthodontic
Regulation Number: 872.5470
Classification Product Code: NJM
Date Received: 01/22/2020
Decision Date: 02/21/2020
Regulation Medical Specialty: Dental
Device Name: LightForce Orthodontic System (LFO System)
Manufacturer: LightForce Orthodontics
Device Classification Name: Bracket, Ceramic, Orthodontic
Regulation Number: 872.5470
Classification Product Code: NJM
Date Received: 01/22/2020
Decision Date: 02/21/2020
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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