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Data / Medical devices / Bracket, Metal, Orthodontic / United States

FDA-registered makers of Bracket, Metal, Orthodontic in the United States: 28 establishments

28 establishments in the United States are registered with the FDA to make Bracket, Metal, Orthodontic (product code EJF). 6 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
Bracket, Metal, Orthodontic
Product code
EJF
Country
United States

Makers of Bracket, Metal, Orthodontic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
American OrthodonticsSheboygan, WI, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler2July 30, 1992000api.fda.gov
Azure Microdynamics, Inc.Foothill Ranch, CA, United StatesManufacturer1January 26, 1994000api.fda.gov
CDB CorporationLeland, NC, United StatesManufacturer, Repackager or relabeler1July 30, 1992000api.fda.gov
G & H Wire CompanyFranklin, IN, United StatesComplaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler1July 30, 1992000api.fda.gov
Ortho Organizers, Inc.Savannah, GA, United StatesManufacturer, Repackager or relabeler, Specification developer1July 30, 1992010api.fda.gov
Ortho-Cycle Co.Hollywood, FL, United StatesReprocessor1November 27, 1991000api.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
Allesee Orthodontic Appliances, Inc.Sturtevant, WI, United StatesComplaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Boch Group LLCBurlington, CT, United StatesSpecification developer0000api.fda.gov
CelebraceColleyville, TX, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Dickerson OrthodonticsPhoenix, AZ, 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 StatesManufacturer0000api.fda.gov
Lorelli Technologies LLCFountain Valley, CA, United StatesManufacturer0000api.fda.gov
LightForce OrthodonticsWilmington, MA, United StatesManufacturer0000api.fda.gov
Ormco CorporationPomona, CA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Ormco CorporationBrea, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Ortho Traction PadsNorwalk, CT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Progressive Orthodontics USAAliso Viejo, CA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
RmoFranklin, IN, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
SKY DENT Corp for dental tradingNew York, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Solventum Orthodontics CorporationMonrovia, CA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Solventum US LLCIrvine, CA, United StatesContract manufacturer0000api.fda.gov
TP Orthodontics, Inc.La Porte, IN, United StatesManufacturer0000api.fda.gov
The American Angle, LLCBrooklyn, NY, United StatesContract manufacturer, Specification developer0000api.fda.gov
World Class Technology CorporationMcminnville, OR, United StatesManufacturer0000api.fda.gov
Xemax Surgical Products, Inc.Napa, CA, United StatesComplaint file establishment, Manufacturer, 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.