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Data / Medical devices / Activator, Ultraviolet, For Polymerization / United States

FDA-registered makers of Activator, Ultraviolet, For Polymerization in the United States: 18 establishments

18 establishments in the United States are registered with the FDA to make Activator, Ultraviolet, For Polymerization (product code EBZ). 15 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Activator, Ultraviolet, For Polymerization
Product code
EBZ
Country
United States

Makers of Activator, Ultraviolet, For Polymerization in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ultradent Products Inc.South Jordan, UT, United StatesManufacturer6February 22, 2022000api.fda.gov
Den-Mat Holdings, LLCLompoc, CA, United StatesComplaint file establishment, Manufacturer3November 21, 2008000api.fda.gov
Coltene/Whaledent Inc.Cuyahoga Falls, OH, United StatesContract manufacturer, Manufacturer, Specification developer2November 27, 2012000api.fda.gov
Dentlight Inc.Plano, TX, United StatesManufacturer2April 19, 2019000api.fda.gov
Dentsply LLCMilford, DE, United StatesManufacturer, Specification developer2November 20, 2019000api.fda.gov
Kerr CorporationOrange, CA, United StatesComplaint file establishment, Specification developer2July 18, 2017000api.fda.gov
Addent, Inc.Danbury, CT, United StatesManufacturer1June 23, 2006000api.fda.gov
Allure OrthoWhitinsville, MA, United StatesSpecification developer1September 16, 2022000api.fda.gov
Cao Group, Inc.W Jordan, UT, United StatesManufacturer, Manufacturer for export1June 12, 2006000api.fda.gov
Garrison Dental SolutionsSpring Lake, MI, United StatesComplaint file establishment, Specification developer1August 1, 2024000api.fda.gov
Handpiece Headquarters - HPR Inc.Placentia, CA, United StatesSpecification developer1November 2, 2023010api.fda.gov
Inter-Med, Inc.Racine, WI, United StatesSpecification developer1June 8, 2017000api.fda.gov
Parkell, Inc.Edgewood, NY, United StatesManufacturer1November 28, 2006000api.fda.gov
Spring Health Products, Inc.Norristown, PA, United StatesManufacturer1September 29, 1999000api.fda.gov
Solventum Orthodontics CorporationMonrovia, CA, United StatesComplaint file establishment, Manufacturer, Specification developer1May 16, 2001000api.fda.gov
Asi Medical, Inc.Englewood, CO, United StatesManufacturer0000api.fda.gov
Miller Technical ServicesPlymouth, MI, United StatesContract manufacturer0000api.fda.gov
Proguard Health Inc.Los Angeles, 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.