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Data / Medical devices / Mask, Scavenging / United States

FDA-registered makers of Mask, Scavenging in the United States: 9 establishments

9 establishments in the United States are registered with the FDA to make Mask, Scavenging (product code KHA). 1 has 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
Mask, Scavenging
Product code
KHA
Country
United States

Makers of Mask, Scavenging in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Accutron, Inc.Phoenix, AZ, United StatesManufacturer1March 28, 1997000api.fda.gov
Bags And Wraps Etc., Inc.Honolulu, HI, United StatesSpecification developer0000api.fda.gov
Ecoguard IncGrover, NC, United StatesContract manufacturer, Manufacturer0000api.fda.gov
ICU Eyecare Solutions Inc.Hollister, CA, United StatesManufacturer0000api.fda.gov
Injection Safety Industries LLCBowling Green, KY, United StatesSpecification developer0000api.fda.gov
Laguna ScientificAliso Viejo, CA, United StatesSpecification developer0000api.fda.gov
Obbomed Group LLCPomona, CA, United StatesSpecification developer0000api.fda.gov
Precision Fluidics Division Parker Hannifin Corp.Hatfield, PA, United StatesManufacturer, Specification developer0000api.fda.gov
Safer Medical ProductsFircrest, WA, 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.