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Data / Medical devices / Apparatus, Exhaust, Surgical / United States

FDA-registered makers of Apparatus, Exhaust, Surgical in the United States: 25 establishments

25 establishments in the United States are registered with the FDA to make Apparatus, Exhaust, Surgical (product code FYD). 18 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

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Device
Apparatus, Exhaust, Surgical
Product code
FYD
Country
United States

Makers of Apparatus, Exhaust, Surgical in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
ConMed CorporationGreenwood Village, CO, United StatesSpecification developer11August 5, 2024000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesManufacturer4March 3, 2014000api.fda.gov
I.C. Medical, Inc.Phoenix, AZ, United StatesManufacturer4October 30, 2017000api.fda.gov
CovidienBoulder, CO, United StatesManufacturer, Repackager or relabeler3January 14, 2015000api.fda.gov
CovidienLafayette, CO, United StatesSpecification developer2January 14, 2015000api.fda.gov
Stryker InstrumentsPortage, MI, United StatesComplaint file establishment, Specification developer2February 7, 2019000api.fda.gov
Acuderm, Inc.Fort Lauderdale, FL, United StatesManufacturer1February 9, 1994000api.fda.gov
Ethicon Endo-Surgery, Inc.Cincinnati, OH, United StatesSpecification developer1June 26, 2020000api.fda.gov
Ethicon Endo-Surgery, LLCGuaynabo, PR, United StatesSpecification developer1June 26, 2020000api.fda.gov
Global Life Sciences Solutions USA LLCMarlborough, MA, United StatesComplaint file establishment, Specification developer1August 20, 1999000api.fda.gov
Medgyn Products, Inc.Westmont, IL, United StatesManufacturer1August 12, 1991000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer1January 3, 2022000api.fda.gov
Megadyne Medical Products, Inc.Cincinnati, OH, United StatesSpecification developer1June 26, 2020000api.fda.gov
Medrange CorporationBrea, CA, United StatesSpecification developer1April 10, 2024000api.fda.gov
Medtronic Distribution CenterMemphis, TN, United StatesManufacturer1June 29, 1998000api.fda.gov
Northgate Technologies Inc.Elgin, IL, United StatesComplaint file establishment, Manufacturer1March 25, 2021000api.fda.gov
SurgiSmoke SolutionsSaint Paul, MN, United StatesComplaint file establishment, Specification developer1September 28, 1989010api.fda.gov
Utah Medical Products, Inc.Midvale, UT, United StatesManufacturer1August 28, 1995000api.fda.gov
Armm, Inc.Huntington Beach, CA, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
Jabil Inc.Auburn Hills, MI, United StatesContract manufacturer0000api.fda.gov
Stryker Manufacturing KalamazooPortage, MI, United StatesContract manufacturer0000api.fda.gov
Syntech, Int'l Inc.Irvine, CA, United StatesContract manufacturer0000api.fda.gov
Tessy Plastics Corp.Elbridge, NY, United StatesContract manufacturer0000api.fda.gov
Ultraviolet Devices, Inc.Valencia, CA, United StatesContract manufacturer0000api.fda.gov
Vaupell Midwest Molding and ToolingConstantine, MI, United StatesContract 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.