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Data / Medical devices / Adaptor, Hygiene / United States

FDA-registered makers of Adaptor, Hygiene in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Adaptor, Hygiene (product code ILS). 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
Adaptor, Hygiene
Product code
ILS
Country
United States

Makers of Adaptor, Hygiene in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
ASP Global, LLCAustell, GA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Agiliti Health - HaysHays, KS, United StatesManufacturer0000api.fda.gov
Altimate Medical, Inc.Frankfort, IL, United StatesManufacturer0000api.fda.gov
Bruce Medical SupplyWaltham, MA, United StatesManufacturer0000api.fda.gov
Community Medical Products LLCPrairie du Sac, WI, United StatesSpecification developer0000api.fda.gov
Cross Innovations LLCCheyenne, WY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Dignity Lifts LLCClarkston, MI, United StatesSpecification developer0000api.fda.gov
Eagle Health SuppliesOrange, CA, United StatesSpecification developer0000api.fda.gov
GF Health Products, IncAtlanta, GA, United StatesManufacturer0010api.fda.gov
Horst Enterprises IncSaint Petersburg, FL, United StatesSpecification developer0000api.fda.gov
Inovo Inc.Lehigh Acres, FL, United StatesManufacturer0000api.fda.gov
Liftseat CorporationOak Brook, IL, United StatesSpecification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Merchsource LLCIrvine, CA, United StatesSpecification developer0000api.fda.gov
Metal Components, LLCPlainwell, MI, United StatesContract manufacturer0000api.fda.gov
Nova Ortho-Med, Inc.North Aurora, IL, United StatesSpecification developer0000api.fda.gov
P.C.P. ChampionRipley, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Performance Health Supply, LLC.Cedarburg, WI, United StatesSpecification developer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
Richardson Products, Inc.Frankfort, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Sunrise Medical (US) LLCMount Juliet, TN, United StatesManufacturer0000api.fda.gov
Tumble Forms, Inc.Dolgeville, NY, United StatesContract manufacturer0000api.fda.gov
Unite Medical, LLCLithia Springs, GA, 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.