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Data / Medical devices / Source, Carrier, Fiberoptic Light / United States

FDA-registered makers of Source, Carrier, Fiberoptic Light in the United States: 22 establishments

22 establishments in the United States are registered with the FDA to make Source, Carrier, Fiberoptic Light (product code EQH). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Source, Carrier, Fiberoptic Light
Product code
EQH
Country
United States

Makers of Source, Carrier, Fiberoptic Light in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Integra LifeSciences CorporationPrinceton, NJ, United StatesComplaint file establishment, Specification developer1May 22, 1987000api.fda.gov
Integra LifeSciences Production CorporationMansfield, MA, United StatesManufacturer1May 22, 1987000api.fda.gov
Linvatec CorporationLargo, FL, United StatesManufacturer, Specification developer1May 22, 1987000api.fda.gov
Acclarent, Inc.Irvine, CA, United StatesSpecification developer0000api.fda.gov
Arthrex, Inc.Naples, FL, United StatesSpecification developer0000api.fda.gov
Arthrex Manufacturing Inc.Pendleton, SC, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
Arthrex, Inc.Ave Maria, FL, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
Bear-Ent, LLCMalvern, PA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Elmed, Inc.Glendale Heights, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Eusa Global LLCMedley, FL, United StatesContract manufacturer0000api.fda.gov
Fiberoptics Technology, Inc.Pomfret, CT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Harwood Design, Inc.Bristol, PA, United StatesContract manufacturer0000api.fda.gov
Hosmed Inc.Doral, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Innomed, Inc.Savannah, GA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Ondine Research Laboratories/Ondine Biomedical Inc. (us)Bothell, WA, United StatesComplaint file establishment, Manufacturer for export, Repackager or relabeler, Specification developer0000api.fda.gov
Phoenix Instruments, Inc.Lisle, IL, United StatesContract manufacturer0000api.fda.gov
Schott North America Inc - Lighting And ImagingSouthbridge, MA, United StatesManufacturer, Specification developer0000api.fda.gov
Stryker EndoscopySan Jose, CA, United StatesManufacturer0000api.fda.gov
Sunoptic Technologies, LLCJacksonville, FL, United StatesManufacturer0000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Weco Manufacturing Group-HenriettaRochester, NY, United StatesManufacturer, 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.