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Data / Medical devices / Port & Catheter, Implanted, Subcutaneous, Intravascular / United States

FDA-registered makers of Port & Catheter, Implanted, Subcutaneous, Intravascular in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Port & Catheter, Implanted, Subcutaneous, Intravascular (product code LJT). 15 have a 510(k) clearance or PMA approval on file and 5 have a recall event. FDA data exported November 3, 2026.

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Device
Port & Catheter, Implanted, Subcutaneous, Intravascular
Product code
LJT
Country
United States

Makers of Port & Catheter, Implanted, Subcutaneous, Intravascular in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Bard Access Systems, Inc.Salt Lake City, UT, United StatesComplaint file establishment, Specification developer23September 5, 2025040api.fda.gov
Angiodynamics, Inc.Queensbury, NY, United StatesManufacturer19May 22, 2020010api.fda.gov
AngioDynamics, Inc.Marlborough, MA, United StatesSpecification developer19May 22, 2020000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer9May 21, 2015010api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesComplaint file establishment, Specification developer7March 1, 2010000api.fda.gov
Medical Components IncHarleysville, PA, United StatesComplaint file establishment, Manufacturer, Specification developer7March 15, 2016080api.fda.gov
PFM Medical, IncCarlsbad, CA, United StatesComplaint file establishment, Specification developer5July 16, 2013000api.fda.gov
Norfolk Medical Products, Inc.Skokie, IL, United StatesManufacturer3October 27, 2011000api.fda.gov
Arrow International, LLC (subsidiary of Teleflex Incorporated)Wyomissing, PA, United StatesSpecification developer1October 27, 2000010api.fda.gov
CovidienNorth Haven, CT, United StatesManufacturer1August 10, 1995000api.fda.gov
Medtronic NeurosurgeryFort Worth, TX, United StatesSpecification developer1July 14, 1994000api.fda.gov
Portal Access IncMiami Beach, FL, United StatesComplaint file establishment, Specification developer1June 17, 2026000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler1October 27, 2000000api.fda.gov
Vygon UsaLansdale, PA, United StatesSpecification developer1December 11, 2013000api.fda.gov
Vygon MFGDover, NH, United StatesManufacturer1December 11, 2013000api.fda.gov
Cook IncorporatedEllettsville, IN, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
EPIC MedTec OEM Catheter & Wire LLCPlymouth, MN, United StatesContract manufacturer0000api.fda.gov
IntriCon Corporation VHVadnais Heights, MN, United StatesContract manufacturer0000api.fda.gov
Primrose Medical, Inc.East Walpole, MA, United StatesManufacturer0000api.fda.gov
Primo Medical Group, INCStoughton, MA, United StatesContract manufacturer, Manufacturer for export0000api.fda.gov
Sterilization Services Of Georgia, Inc.Atlanta, GA, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov

Updated November 3, 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.