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Data / Medical devices / Apron, Protective / United States

FDA-registered makers of Apron, Protective in the United States: 14 establishments

14 establishments in the United States are registered with the FDA to make Apron, Protective (product code IWO). 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
Apron, Protective
Product code
IWO
Country
United States

Makers of Apron, Protective in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Alimed, LLCDedham, MA, United StatesSpecification developer0000api.fda.gov
Burlington Medical, LLCNewport News, VA, United StatesManufacturer0010api.fda.gov
Infab, LLC.Camarillo, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Palmero Healthcare LLCNorthbrook, IL, United StatesManufacturer0000api.fda.gov
Protech Leaded Eyewear, Inc.West Palm Beach, FL, United StatesContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
RF Design, Inc.Howell, MI, United StatesManufacturer0000api.fda.gov
Salus Scientific CorpCharleston, SC, United StatesManufacturer0000api.fda.gov
Shielding Intl., Inc.Madras, OR, United StatesManufacturer0000api.fda.gov
Techno-Aide, Inc.Whites Creek, TN, United StatesManufacturer0000api.fda.gov
Trivitron Imaging Solutions IncScottsboro, AL, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Two One Two New York, Inc.Edgewood, NY, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Wolf X-Ray CorpBattleboro, NC, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Worldwide Innovations & Technologies, Inc.Lenexa, KS, 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.