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Data / Medical devices / Heat Source For Bleaching Teeth / United States

FDA-registered makers of Heat Source For Bleaching Teeth in the United States: 14 establishments

14 establishments in the United States are registered with the FDA to make Heat Source For Bleaching Teeth (product code EEG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Heat Source For Bleaching Teeth
Product code
EEG
Country
United States

Makers of Heat Source For Bleaching Teeth in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Addent, Inc.Danbury, CT, United StatesManufacturer0000api.fda.gov
Andersonbrecon Inc.Rockford, IL, United StatesContract manufacturer0000api.fda.gov
Beaming White LLCVancouver, WA, United StatesManufacturer0000api.fda.gov
Cao Group, Inc.W Jordan, UT, United StatesManufacturer0000api.fda.gov
Colgate-Palmolive CompanyPiscataway, NJ, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Discus Dental, LLCOntario, CA, United StatesManufacturer0000api.fda.gov
GLO Science, Inc.Garden Grove, CA, United StatesComplaint file establishment, Contract manufacturer, Specification developer0000api.fda.gov
Kmi Imi Group / Dba: Innovative Med, Inc.Irvine, CA, United StatesManufacturer0000api.fda.gov
Moon Oral Care, LLC.El Segundo, CA, United StatesSpecification developer0000api.fda.gov
Nanova Biomaterials IncColumbia, MO, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Novaalab LLCWilmington, DE, United StatesSpecification developer0000api.fda.gov
Philips Oral Healthcare, LLCBothell, WA, United StatesSpecification developer0000api.fda.gov
Procter & Gamble Co., Regulatory AffairsMason, OH, United StatesSpecification developer0000api.fda.gov
T33 Dental Inc.Cambridge, MA, United StatesComplaint file establishment, 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.