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Data / Medical devices / Camera, Cine, Endoscopic, Without Audio / United States

FDA-registered makers of Camera, Cine, Endoscopic, Without Audio in the United States: 9 establishments

9 establishments in the United States are registered with the FDA to make Camera, Cine, Endoscopic, Without Audio (product code FWL). 0 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
Camera, Cine, Endoscopic, Without Audio
Product code
FWL
Country
United States

Makers of Camera, Cine, Endoscopic, Without Audio in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Arthrex Logistic CenterFort Myers, FL, United StatesManufacturer0000api.fda.gov
Firefly GlobalBelmont, MA, United StatesManufacturer0000api.fda.gov
Hosmed Inc.Doral, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Novaprobe Inc.Lansdale, PA, United StatesManufacturer0000api.fda.gov
Perioview, LLCSurprise, AZ, United StatesManufacturer0000api.fda.gov
Pure Novamed IncLong Beach, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Stryker Corp.Kalamazoo, MI, United StatesContract manufacturer0000api.fda.gov
Stryker Manufacturing KalamazooPortage, MI, United StatesContract manufacturer0000api.fda.gov
Taevas Life Sciences IncPrinceton, NJ, 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.