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Data / Medical devices / Adhesive, Bracket And Tooth Conditioner, Resin / United States

FDA-registered makers of Adhesive, Bracket And Tooth Conditioner, Resin in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Adhesive, Bracket And Tooth Conditioner, Resin (product code DYH). 17 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
Adhesive, Bracket And Tooth Conditioner, Resin
Product code
DYH
Country
United States

Makers of Adhesive, Bracket And Tooth Conditioner, Resin in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Reliance Orthodontic Products, Inc.Itasca, IL, United StatesManufacturer for export, Repackager or relabeler, Specification developer22April 27, 2020000api.fda.gov
Ormco CorporationPomona, CA, United StatesComplaint file establishment, Specification developer9January 3, 2025000api.fda.gov
Ormco CorporationBrea, CA, United StatesComplaint file establishment, Specification developer9January 3, 2025000api.fda.gov
American OrthodonticsSheboygan, WI, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler8June 3, 2026000api.fda.gov
Solventum Orthodontics CorporationMonrovia, CA, United StatesComplaint file establishment, Manufacturer, Specification developer7December 22, 2023000api.fda.gov
Scientific Pharmaceuticals, Inc.Pomona, CA, United StatesContract manufacturer, Manufacturer6July 21, 2000000api.fda.gov
GC America Inc.Alsip, IL, United StatesManufacturer, Repackager or relabeler5June 11, 2008000api.fda.gov
Ultradent Products Inc.South Jordan, UT, United StatesManufacturer, Repackager or relabeler4September 7, 2011000api.fda.gov
Dental Technologies, Inc.Lincolnwood, IL, United StatesManufacturer3August 10, 1994000api.fda.gov
Pulpdent CorporationWatertown, MA, United StatesManufacturer2July 14, 1995000api.fda.gov
Solventum US LLCIrvine, CA, United StatesContract manufacturer, Manufacturer2December 22, 2023000api.fda.gov
TP Orthodontics, Inc.La Porte, IN, United StatesManufacturer2October 14, 2022000api.fda.gov
Zest Anchors, LLCCarlsbad, CA, United StatesRepackager or relabeler, Specification developer2March 18, 2015000api.fda.gov
Bisco, Inc.Schaumburg, IL, United StatesContract manufacturer, Manufacturer1February 7, 2012000api.fda.gov
Prime Dental Manufacturing, Inc.Chicago, IL, United StatesContract manufacturer, Manufacturer1October 24, 2001000api.fda.gov
Solventum Us LLCEagan, MN, United StatesManufacturer1December 22, 2023000api.fda.gov
Solventum US LLCSan Antonio, TX, United StatesSpecification developer1May 29, 1991000api.fda.gov
Den-Mat Holdings, LLCLompoc, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Kerr CorporationOrange, CA, United StatesContract manufacturer0000api.fda.gov
Kerr CorporationPomona, CA, United StatesContract manufacturer0000api.fda.gov
Premier Dental Products Co.Plymouth Meeting, PA, United StatesComplaint file establishment, Specification developer0000api.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.