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Data / Medical devices / Electrocautery, Gynecologic (And Accessories) / United States

FDA-registered makers of Electrocautery, Gynecologic (And Accessories) in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Electrocautery, Gynecologic (And Accessories) (product code HGI). 13 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Electrocautery, Gynecologic (And Accessories)
Product code
HGI
Country
United States

Makers of Electrocautery, Gynecologic (And Accessories) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Coopersurgical, Inc.Trumbull, CT, United StatesManufacturer, Repackager or relabeler6October 20, 2006070api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer3January 3, 2014000api.fda.gov
Conmed CorporationUtica, NY, United StatesComplaint file establishment, Manufacturer2September 27, 1994000api.fda.gov
ConMed CorporationGreenwood Village, CO, United StatesSpecification developer2September 27, 1994000api.fda.gov
Liger MedicalLehi, UT, United StatesManufacturer2April 23, 2021000api.fda.gov
Omni-Guide Holdings, Inc.Billerica, MA, United StatesManufacturer2January 3, 2014000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler2March 21, 1995000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer2March 21, 1995000api.fda.gov
Gyrus ACMI, Inc.Brooklyn Park, MN, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer1March 21, 1995000api.fda.gov
Medgyn Products, Inc.Westmont, IL, United StatesManufacturer, Manufacturer for export1November 1, 2002000api.fda.gov
Megadyne Medical Products, Inc.Cincinnati, OH, United StatesSpecification developer1June 27, 1994000api.fda.gov
Premier Dental Products Co.Plymouth Meeting, PA, United StatesSpecification developer1February 1, 2001000api.fda.gov
Utah Medical Products, Inc.Midvale, UT, United StatesManufacturer, Specification developer1September 18, 1991000api.fda.gov
Ethicon Endo-Surgery, Inc.Cincinnati, OH, United StatesSpecification developer0000api.fda.gov
Ethicon Endo-Surgery, LLCGuaynabo, PR, United StatesSpecification developer0000api.fda.gov
Geotec, Inc.Warwick, RI, United StatesContract manufacturer0000api.fda.gov
Grace Manufacturing IncRussellville, AR, United StatesManufacturer0000api.fda.gov
Jabil Inc.Auburn Hills, MI, United StatesContract manufacturer0000api.fda.gov
Linemaster Switch Corp.Woodstock, CT, United StatesContract manufacturer0000api.fda.gov
Modo IncHillsboro, OR, United StatesContract manufacturer0000api.fda.gov
Modo, Inc.McMinnville, OR, United StatesContract manufacturer0000api.fda.gov
Nypro Healthcare Baja Inc. (Albuquerque)Albuquerque, NM, United StatesContract manufacturer, Contract sterilizer0000api.fda.gov
Plexus Corp.Neenah, WI, United StatesContract manufacturer0000api.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.