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Data / Medical devices / Tube, Aspirating, Flexible, Connecting / United States

FDA-registered makers of Tube, Aspirating, Flexible, Connecting in the United States: 31 establishments

31 establishments in the United States are registered with the FDA to make Tube, Aspirating, Flexible, Connecting (product code BYY). 2 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
Tube, Aspirating, Flexible, Connecting
Product code
BYY
Country
United States

Makers of Tube, Aspirating, Flexible, Connecting in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Conmed CorporationUtica, NY, United StatesComplaint file establishment, Manufacturer1June 2, 1978000api.fda.gov
Conmed CorporationWestborough, MA, United StatesSpecification developer1June 2, 1978000api.fda.gov
Armm, Inc.Huntington Beach, CA, United StatesContract manufacturer, Contract sterilizer, Manufacturer0000api.fda.gov
Allied Medical LLCEarth City, MO, United StatesManufacturer0000api.fda.gov
B. Braun Medical Inc.Bethlehem, PA, United StatesSpecification developer0000api.fda.gov
Black & Black Surgical, Inc.Tucker, GA, United StatesSpecification developer0000api.fda.gov
Busse Hospital DisposablesHauppauge, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Bausch & Lomb IncorporatedManchester, MO, United StatesManufacturer0000api.fda.gov
Centurion Medical Products, LPHowell, MI, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
CHS USA IncorporatedPeachtree City, GA, United StatesSpecification developer0000api.fda.gov
Clinical Innovations, LLCMurray, UT, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Deroyal Industries, Inc.New Tazewell, TN, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
Drive Northpoint, LLCPalmetto, GA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Gilero, IncPittsboro, NC, United StatesContract manufacturer0000api.fda.gov
Icu Medical, Inc.Lake Forest, IL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Medgyn Products, Inc.Westmont, IL, United StatesManufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Micro Therapeutics, Inc. Dba Ev3 NeurovascularIrvine, CA, United StatesSpecification developer0000api.fda.gov
Micro Therapeutics, Inc. Dba Ev3 NeurovascularIrvine, CA, United StatesManufacturer0000api.fda.gov
Microtek Medical LLCEagan, MN, United StatesSpecification developer0000api.fda.gov
NDH Medical, Inc.Saint Petersburg, FL, United StatesContract manufacturer0000api.fda.gov
Nico CorporationIndianapolis, IN, United StatesSpecification developer0000api.fda.gov
Phoenix Instruments, Inc.Lisle, IL, United StatesContract manufacturer0000api.fda.gov
Tobra Medical, Inc.Raleigh, NC, United StatesComplaint file establishment, Specification developer0000api.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
U.S. Surgitech, Inc.Carol Stream, IL, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Vayuclear IncCharleston, SC, United StatesSpecification developer0000api.fda.gov
Zien Medical Technologies LLCSalt Lake City, UT, 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.