Data / Medical devices / United States / Led Technologies, Inc.
Led Technologies, Inc.: FDA-registered device maker in Largo, FL, United States, 10 510(k) clearances
Led Technologies, Inc. is registered with the FDA (registration 3015974280) in Largo, FL, United States. It lists 4 device types. The FDA files 10 510(k) clearances under its listings, the newest dated December 21, 2022. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3015974280
- FEI number
- 3012420078
- Address
- 11701 Belcher Rd S., Suite 110, Largo, FL, United States, 33773
- Owner or operator
- LED Technologies, Inc. (10028128)
- Roles
- Manufacturer
- First device listed
- December 19, 2016
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Eraser, Dental Stain | MAU | 1 | Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer | accessdata.fda.gov |
| Over-The-Counter Powered Light Based Laser For Acne | OLP | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 21, 2022 | K223482 | reVive Light Therapy® Wrinkle and Acne LED Device | OHS | Substantially Equivalent | Led Technologies, Inc. | accessdata.fda.gov |
| July 27, 2022 | K221430 | reVive Light Therapy LED Cleansing System | OHS | Substantially Equivalent | Led Technologies, Inc. | accessdata.fda.gov |
| December 21, 2021 | K210968 | reVive Light Therapy Essentials | OLP | Substantially Equivalent | Led Technologies, Inc. | accessdata.fda.gov |
| March 14, 2019 | K183247 | dpl Faceware | OHS | Substantially Equivalent | Led Technologies, Inc. | accessdata.fda.gov |
| February 7, 2019 | K183118 | dpl SpotLite | OLP | Substantially Equivalent | Led Technologies, Inc. | accessdata.fda.gov |
| June 4, 2018 | K180447 | reVive Light Therapy LED Cleansing System | OLP | Substantially Equivalent | Led Technologies, Inc. | accessdata.fda.gov |
| May 15, 2018 | K180445 | reVive Light Therapy LED Ultrasonic Wrinkle System | OHS | Substantially Equivalent | Led Technologies, Inc. | accessdata.fda.gov |
| April 3, 2018 | K180320 | dpl IIa Panel | OHS | Substantially Equivalent | Led Technologies, Inc. | accessdata.fda.gov |
| January 9, 2018 | K172662 | reVive Perioral | OHS | Substantially Equivalent | Led Technologies, Inc. | accessdata.fda.gov |
| August 7, 2017 | K171386 | dpl SpectraLite | OHS | Substantially Equivalent | Led Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Over-The-Counter Powered Light Based Laser For Acne
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Eraser, Dental Stain
Updated December 21, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.