Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

dpl SpotLite

K-Number: K183118 · 2019-02-07

ApplicantLed Technologies, Inc.
Decision Date2019-02-07
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

dpl SpotLite is a medical device manufactured by Led Technologies, Inc.. It received FDA 510(k) clearance on 2019-02-07 under approval number K183118. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the dpl SpotLite?

dpl SpotLite is a medical device that received FDA 510(k) clearance on 2019-02-07. It is manufactured by Led Technologies, Inc.. The 510(k) number is K183118.

When was dpl SpotLite approved by the FDA?

dpl SpotLite received FDA 510(k) clearance on 2019-02-07, under approval number K183118.

What company makes dpl SpotLite?

dpl SpotLite is manufactured by Led Technologies, Inc..

What is the FDA product code for dpl SpotLite?

The FDA product code for dpl SpotLite is OLP.

Other Devices by Led Technologies, Inc.

K171386dpl SpectraLite K171390dpl II Panel K180447reVive Light Therapy LED Cleansing System K180445reVive Light Therapy LED Ultrasonic Wrinkle System K180320dpl IIa Panel K172662reVive Perioral

View all 12 devices →

Related Devices (Code: OLP)

K162371Pulsaderm ACE-All BlueNutra Luxe MD, LLC K162450ESPADA Acne-Clearing Blue Light PenForeo, Inc. K161941Pulsaderm Acne DeviceNutra Luxe MD, LLC K160691Acne Light Therapy WandZuko, Inc. K160821Tria SapphireTria Beauty, Inc. K153081Clear Bi-LightMichael Todd, LP

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑