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Data / Medical devices / Retainer, Screw Expansion, Orthodontic / United States

FDA-registered makers of Retainer, Screw Expansion, Orthodontic in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Retainer, Screw Expansion, Orthodontic (product code DYJ). 0 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
Retainer, Screw Expansion, Orthodontic
Product code
DYJ
Country
United States

Makers of Retainer, Screw Expansion, Orthodontic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Alta Smiles, LLCFort Washington, PA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
American OrthodonticsSheboygan, WI, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Apnomed, Inc.Bellevue, WA, United StatesSpecification developer0000api.fda.gov
Aurum Ceramic Dental Laboratories LLCSpokane, WA, United StatesManufacturer0000api.fda.gov
Aegis Star Dental Technologies IncBoston, MA, United StatesManufacturer0000api.fda.gov
Allesee Orthodontic Appliances, Inc.Sturtevant, WI, United StatesComplaint file establishment, Manufacturer, Specification developer0010api.fda.gov
DR Douglas J Shilliday IncColumbus, OH, United StatesManufacturer, Specification developer0000api.fda.gov
Five Star Orthodontic Laboratory & Supply, Inc.Denton, TX, United StatesManufacturer0000api.fda.gov
GC Orthodontics America Inc.Alsip, IL, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Great Lakes Dental Technologies, Ltd.Tonawanda, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
KTJ Dental Lab IncLos Angeles, CA, United StatesManufacturer0000api.fda.gov
Ortho Organizers, Inc.Savannah, GA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Palaxa Precision LLCNewport, MN, United StatesSpecification developer0000api.fda.gov
RICOmed ManufacturingRichardson, TX, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
RmoFranklin, IN, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Sprintray Inc.Los Angeles, CA, United StatesManufacturer0000api.fda.gov
Sprintray Inc.Huntington Beach, CA, United StatesManufacturer, Specification developer0000api.fda.gov
TP Orthodontics, Inc.La Porte, IN, United StatesManufacturer0000api.fda.gov
Vivos Therapeutics INC.Murray, KY, United StatesSpecification developer0000api.fda.gov
Xplora USA LLCCarrollton, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
proNet, A Division Desco Industries Inc.Anaheim, CA, United StatesContract manufacturer, Repackager or relabeler0000api.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.