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Data / Medical devices / Apparatus, Suction, Operating-Room, Wall Vacuum Powered / United States

FDA-registered makers of Apparatus, Suction, Operating-Room, Wall Vacuum Powered in the United States: 55 establishments

55 establishments in the United States are registered with the FDA to make Apparatus, Suction, Operating-Room, Wall Vacuum Powered (product code GCX). 11 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 3, 2026.

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Device
Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Product code
GCX
Country
United States

Makers of Apparatus, Suction, Operating-Room, Wall Vacuum Powered in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler4July 28, 1993000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer4July 28, 1993000api.fda.gov
Stryker EndoscopySan Jose, CA, United StatesComplaint file establishment, Manufacturer, Specification developer2December 9, 2004050api.fda.gov
Bemis Manufacturing Co.Sheboygan Falls, WI, United StatesManufacturer1December 20, 1977000api.fda.gov
Biomet MicrofixationJacksonville, FL, United StatesManufacturer, Repackager or relabeler1July 25, 1997000api.fda.gov
Coopersurgical, Inc.Trumbull, CT, United StatesManufacturer1April 19, 1991000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer1November 16, 1981000api.fda.gov
Implantech Associates, Inc.Ventura, CA, United StatesManufacturer1January 10, 1994000api.fda.gov
Med Michigan Holdings LLCLake Odessa, MI, United StatesManufacturer1April 17, 1997010api.fda.gov
Sscor, Inc.Simi Valley, CA, United StatesManufacturer, Specification developer1April 25, 1995000api.fda.gov
W.T. Farley, Inc.Ladson, SC, United StatesManufacturer1December 12, 1978000api.fda.gov
Accumedix, Inc.Libertyville, IL, United StatesContract manufacturer0000api.fda.gov
AG Industries LLCFairburn, GA, United StatesManufacturer0000api.fda.gov
Allwin Medical Devices, Inc.Anaheim, CA, United StatesManufacturer0000api.fda.gov
Angiodynamics, Inc.Queensbury, NY, United StatesManufacturer0000api.fda.gov
Aparata MedicalOrlando, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Applied Medical Technology, Inc.Brecksville, OH, United StatesManufacturer0000api.fda.gov
Allied Medical LLCEarth City, MO, United StatesManufacturer0000api.fda.gov
AngioDynamics, Inc.Marlborough, MA, United StatesSpecification developer0000api.fda.gov
Boehringer Laboratories, LLCPhoenixville, PA, United StatesManufacturer0010api.fda.gov
Busse Hospital DisposablesHauppauge, NY, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Cardinal Health 200, LLCJacksonville, TX, United StatesManufacturer0000api.fda.gov
Cardinal Health P.R. 218, Inc.Anasco, PR, United StatesManufacturer0000api.fda.gov
CLR Medical, Inc.Calverton, MD, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Codan Us Corp.Santa Ana, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Conmed CorporationUtica, NY, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
ConMed CorporationGreenwood Village, CO, United StatesSpecification developer0000api.fda.gov
Conmed CorporationWestborough, MA, United StatesSpecification developer0000api.fda.gov
Dechoker LLCWheat Ridge, CO, United StatesManufacturer0000api.fda.gov
Depuy Orthopaedics, Inc.Warsaw, IN, United StatesManufacturer, Specification developer0000api.fda.gov
Depuy Spine, Inc.Raynham, MA, United StatesSpecification developer0000api.fda.gov
Dukal LLCRonkonkoma, NY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Grace Medical, Inc.Memphis, TN, United StatesManufacturer0000api.fda.gov
Grandrapids Foam Technologies, Inc.Grand Rapids, MI, United StatesContract manufacturer0000api.fda.gov
Highridge Medical, LLCWestminster, CO, United StatesSpecification developer0000api.fda.gov
Icu Medical, IncSalt Lake City, UT, United StatesManufacturer0000api.fda.gov
JEDMED Instrument CompanySaint Louis, MO, United StatesManufacturer0000api.fda.gov
Lifeport, LLC.Woodland, WA, United StatesManufacturer0000api.fda.gov
Linvatec CorporationLargo, FL, United StatesSpecification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Olive Branch Distribution CenterOlive Branch, MS, United StatesContract manufacturer0000api.fda.gov
Pilotis Tech LLCBrookhaven, GA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Rico Suction Labs, Inc.Mobile, AL, United StatesManufacturer0000api.fda.gov
Robling Medical, LLCYoungsville, NC, United StatesContract manufacturer0000api.fda.gov
Rockford SpecialtiesLoves Park, IL, United StatesContract manufacturer0000api.fda.gov
Stryker Puerto Rico, LLC.Arroyo, PR, United StatesManufacturer0000api.fda.gov
Small Beginnings Inc.Hesperia, CA, United StatesSpecification developer0000api.fda.gov
Stryker InstrumentsPortage, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Suction Switch, LLCLafayette, LA, United StatesManufacturer0000api.fda.gov
SunMed Group Holdings, LLCGrand Rapids, MI, United StatesSpecification developer0000api.fda.gov
Trimedyne, Inc.Corona, CA, United StatesManufacturer, Specification developer0000api.fda.gov
Thunderbird Molding GreensboroGreensboro, NC, United StatesContract manufacturer0000api.fda.gov
Viseon, Inc.Irvine, CA, United StatesManufacturer0000api.fda.gov
Westmed, Inc.Tucson, AZ, United StatesContract manufacturer, Manufacturer0000api.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.