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Data / Medical devices / Trocar / United States

FDA-registered makers of Trocar in the United States: 24 establishments

24 establishments in the United States are registered with the FDA to make Trocar (product code DRC). 5 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers of this device in the United StatesWatch these makers
Device
Trocar
Product code
DRC
Country
United States

Makers of Trocar in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Pressure Products Medical Device Manufacturing LLCMorton, PA, United StatesManufacturer7May 17, 2024000api.fda.gov
Argon Medical Devices Inc.Athens, TX, United StatesContract manufacturer, Manufacturer, Repackager or relabeler2April 6, 1998000api.fda.gov
Synaptic Medical CorporationCarlsbad, CA, United StatesComplaint file establishment, Manufacturer2July 26, 2024000api.fda.gov
Advance Medical Designs, Inc.Marietta, GA, United StatesManufacturer, Repackager or relabeler1November 14, 1989000api.fda.gov
Coopersurgical, Inc.Trumbull, CT, United StatesManufacturer, Specification developer1April 22, 1991010api.fda.gov
A&m Biomedical Inc.Laguna Hills, CA, United StatesContract manufacturer0000api.fda.gov
Angiodynamics, Inc.Queensbury, NY, United StatesManufacturer0000api.fda.gov
Argon Medical Devices, Inc.Wheeling, IL, United StatesContract manufacturer0000api.fda.gov
AngioDynamics, Inc.Marlborough, MA, United StatesSpecification developer0000api.fda.gov
Busse Hospital DisposablesHauppauge, NY, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer0031api.fda.gov
Indian Wells Medical, Inc.Lake Forest, CA, United StatesManufacturer0000api.fda.gov
Lone Star Medical ProductsStafford, TX, United StatesContract manufacturer0010api.fda.gov
Medical Components IncHarleysville, PA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Merit Medical Systems, Inc.South Jordan, UT, United StatesManufacturer, Specification developer0020api.fda.gov
Merit Medical Systems, Inc.Houston, TX, United StatesContract manufacturer0000api.fda.gov
Needle Specialty ProductsBoyle, MS, United StatesContract manufacturer0000api.fda.gov
Sabin CorporationBlmgtn, IN, United StatesContract manufacturer0000api.fda.gov
Sterilization Services Of VirginiaRichmond, VA, United StatesContract manufacturer0000api.fda.gov
St. Jude MedicalRoseville, MN, United StatesManufacturer0000api.fda.gov
St. Jude Medical, Atrial Fibrillation Division, Inc.Minnetonka, MN, United StatesSpecification 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

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.