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Data / Medical devices / Wire, Orthodontic / United States

FDA-registered makers of Wire, Orthodontic in the United States: 32 establishments

32 establishments in the United States are registered with the FDA to make Wire, Orthodontic (product code DZC). 1 has 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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Get makers of this device in the United StatesWatch these makers
Device
Wire, Orthodontic
Product code
DZC
Country
United States

Makers of Wire, Orthodontic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Five Star Orthodontic Laboratory & Supply, Inc.Denton, TX, United StatesContract manufacturer, Manufacturer, Repackager or relabeler4March 31, 1993000api.fda.gov
Acme-Monaco Corp.New Britain, CT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Acme-Monaco Corp.Presque Isle, ME, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Alta Smiles, LLCFort Washington, PA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
American OrthodonticsSheboygan, WI, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Aseptico, Inc.Woodinville, WA, United StatesManufacturer0000api.fda.gov
BRIUS Technologies Inc.Carrollton, TX, United StatesManufacturer0000api.fda.gov
CelebraceColleyville, TX, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Dickerson OrthodonticsPhoenix, AZ, United StatesManufacturer0000api.fda.gov
Dentsply Sirona Orthodontics Inc.Sarasota, FL, United StatesContract manufacturer0000api.fda.gov
Dentsply Sirona Orthodontics Inc.Richardson, TX, United StatesSpecification developer0000api.fda.gov
G & H Wire CompanyFranklin, IN, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0010api.fda.gov
GC Orthodontics America Inc.Alsip, IL, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Gergens Orthodontic LabPhoenix, AZ, United StatesContract manufacturer0000api.fda.gov
Lorelli Technologies LLCFountain Valley, CA, United StatesManufacturer0000api.fda.gov
Matrix Health, Inc.Greenville, SC, United StatesSpecification developer0000api.fda.gov
Ortho Organizers, Inc.Savannah, GA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Ortho-Tain, Inc.Toa Alta, PR, United StatesManufacturer0000api.fda.gov
Ormco CorporationPomona, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Ormco CorporationBrea, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Reliance Orthodontic Products, Inc.Itasca, IL, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
RICOmed ManufacturingRichardson, TX, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
RmoFranklin, IN, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
SKY DENT Corp for dental tradingNew York, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Specialty Appliances, LLCCumming, GA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Solventum Orthodontics CorporationMonrovia, CA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Tangent OrthodonticsFranklin, IN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
TP Orthodontics, Inc.La Porte, IN, United StatesManufacturer0000api.fda.gov
Ultimate Wireforms, Inc.Bristol, CT, United StatesContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
Vivos Therapeutics INC.Murray, KY, United StatesSpecification developer0000api.fda.gov
World Class Technology CorporationMcminnville, OR, United StatesManufacturer0000api.fda.gov
Wire and Cable Specialties, Inc.Coatesville, PA, 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.