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Data / Medical devices / Basin, Emesis / United States

FDA-registered makers of Basin, Emesis in the United States: 36 establishments

36 establishments in the United States are registered with the FDA to make Basin, Emesis (product code FNY). 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
Basin, Emesis
Product code
FNY
Country
United States

Makers of Basin, Emesis in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Advanced Product Solutions Inc.Dothan, AL, United StatesContract manufacturer0000api.fda.gov
Alpha Scientific Corp.Exton, PA, United StatesManufacturer0000api.fda.gov
Argon Medical Devices Inc.Athens, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
ASP Global, LLCAustell, GA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Action PackagingWoodstock, IL, United StatesSpecification developer0000api.fda.gov
Bionix, LLCMaumee, OH, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Bound Tree Medical, LLCGrand Prairie, TX, United StatesManufacturer0000api.fda.gov
C.R. Bard, Inc.Covington, GA, United StatesContract sterilizer, Specification developer0000api.fda.gov
Cardinal Health 200, LLCJacksonville, TX, United StatesManufacturer0000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer0010api.fda.gov
Deroyal Industries, Inc.New Tazewell, TN, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
DeRoyal Industries, Inc.Powell, TN, United StatesContract manufacturer0000api.fda.gov
Healqu, LLCJersey City, NJ, United StatesSpecification developer0000api.fda.gov
Intl. Medsurg Connection, Inc.Schaumburg, IL, United StatesSpecification developer0000api.fda.gov
KLS-Martin L.P.Jacksonville, FL, United StatesSpecification developer0000api.fda.gov
MEDLINE INDUSTRIES - MundeleinMundelein, IL, United StatesManufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - LaredoLaredo, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Medline Industries, LP - SPTWaukegan, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Medegen Medical ProductsGallaway, TN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Nuance Medical, LLCCarlsbad, CA, United StatesManufacturer0000api.fda.gov
NewGen SurgicalSan Rafael, CA, United StatesSpecification developer0000api.fda.gov
Phoenix Instruments, Inc.Lisle, IL, United StatesContract manufacturer0000api.fda.gov
Pilotis Tech LLCBrookhaven, GA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Prime Medical LLCKnoxville, TN, United StatesSpecification developer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
Tri-Tech Forensics, Inc.Leland, NC, 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
The Vollrath Company LLCKiel, WI, United StatesManufacturer0000api.fda.gov
Typenex Medical, LLCChicago, IL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Vollrath Company LLC, TheSheboygan, WI, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Xodus Medical, Inc.New Kensington, PA, 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.