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Data / Medical devices / Clamp, Wire, Orthodontic / United States

FDA-registered makers of Clamp, Wire, Orthodontic in the United States: 19 establishments

19 establishments in the United States are registered with the FDA to make Clamp, Wire, Orthodontic (product code ECN). 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
Clamp, Wire, Orthodontic
Product code
ECN
Country
United States

Makers of Clamp, Wire, Orthodontic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Acme-Monaco Corp.New Britain, CT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Acme-Monaco Corp.Presque Isle, ME, United StatesContract manufacturer, Manufacturer0000api.fda.gov
American OrthodonticsSheboygan, WI, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
GC Orthodontics America Inc.Alsip, IL, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
H & H Co.Hayden, ID, United StatesRemanufacturer, Repackager or relabeler0000api.fda.gov
Inman Orthodontic Laboratories, Inc.Coral Springs, FL, United StatesSpecification developer0000api.fda.gov
Ortho Organizers, Inc.Savannah, GA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Ormco CorporationPomona, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Ormco CorporationBrea, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Reliance Orthodontic Products, Inc.Itasca, IL, United StatesSpecification developer0000api.fda.gov
Specialty Appliances, LLCCumming, GA, United StatesManufacturer, Specification developer0010api.fda.gov
Stoner IncorporatedQuarryville, PA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Solventum Orthodontics CorporationMonrovia, CA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
TP Orthodontics, Inc.La Porte, IN, United StatesManufacturer0000api.fda.gov
The American Angle, LLCBrooklyn, NY, United StatesContract manufacturer, Specification developer0000api.fda.gov
Ultimate Wireforms, Inc.Bristol, CT, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Utah Medical Products And ServicesMurray, UT, United StatesContract manufacturer0000api.fda.gov
Vivos Therapeutics INC.Murray, KY, United StatesSpecification developer0000api.fda.gov
World Class Technology CorporationMcminnville, OR, United StatesManufacturer0000api.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.