Skip to the page

Data / Medical devices / Light, Ultraviolet, Dermatological / United States

FDA-registered makers of Light, Ultraviolet, Dermatological in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Light, Ultraviolet, Dermatological (product code FTC). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Light, Ultraviolet, Dermatological
Product code
FTC
Country
United States

Makers of Light, Ultraviolet, Dermatological in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
The Daavlin Distributing Co.Bryan, OH, United StatesComplaint file establishment, Manufacturer24December 13, 2023040api.fda.gov
Medtek Skin Care, Inc.Hudson Falls, NY, United StatesManufacturer7October 15, 2014000api.fda.gov
Psoria-Shield IncUtica, NY, United StatesManufacturer2March 8, 2023000api.fda.gov
KBD, Inc.North Las Vegas, NV, United StatesSpecification developer1August 6, 1986000api.fda.gov
Radcliffe Watts, LLCMansfield, OH, United StatesComplaint file establishment, Specification developer1March 4, 2026000api.fda.gov
Zerigo Health, Inc.Carlsbad, CA, United StatesSpecification developer1May 23, 2017000api.fda.gov
Spectrum Assembly Inc.Carlsbad, CA, United StatesContract manufacturer0000api.fda.gov

Updated November 2, 2026. 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.