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Data / Medical devices / Spring, Orthodontic / United States

FDA-registered makers of Spring, Orthodontic in the United States: 17 establishments

17 establishments in the United States are registered with the FDA to make Spring, Orthodontic (product code ECO). 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
Spring, Orthodontic
Product code
ECO
Country
United States

Makers of Spring, 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 StatesManufacturer, Repackager or relabeler0000api.fda.gov
G & H Wire CompanyFranklin, IN, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
GC Orthodontics America Inc.Alsip, IL, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Matrix Health, Inc.Greenville, SC, United StatesSpecification developer0000api.fda.gov
Ortho Organizers, Inc.Savannah, GA, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Ormco CorporationPomona, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Ormco CorporationBrea, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Ortho Traction PadsNorwalk, CT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
RmoFranklin, IN, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Solventum Orthodontics CorporationMonrovia, CA, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Tangent OrthodonticsFranklin, IN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
TP Orthodontics, Inc.La Porte, IN, United StatesManufacturer0010api.fda.gov
Ultimate Wireforms, Inc.Bristol, CT, United StatesContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
World Class Technology CorporationMcminnville, OR, United StatesManufacturer0000api.fda.gov
Zalinsky Ortho Parts, LLCCharlotte, NC, United StatesSpecification 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.