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Data / Medical devices / Unit, Electrosurgical, Endoscopic (With Or Without Accessories) / United States

FDA-registered makers of Unit, Electrosurgical, Endoscopic (With Or Without Accessories) in the United States: 28 establishments

28 establishments in the United States are registered with the FDA to make Unit, Electrosurgical, Endoscopic (With Or Without Accessories) (product code KNS). 21 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.

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Device
Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Product code
KNS
Country
United States

Makers of Unit, Electrosurgical, Endoscopic (With Or Without Accessories) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Boston Scientific CorporationMarlborough, MA, United StatesComplaint file establishment, Specification developer12September 3, 2026051api.fda.gov
Boston Scientific CorporationCoventry, RI, United StatesManufacturer, Manufacturer for export11September 3, 2026000api.fda.gov
Wilson-Cook Medical Inc.Winston Salem, NC, United StatesComplaint file establishment, Manufacturer7September 29, 2025060api.fda.gov
Gyrus ACMI, Inc.Brooklyn Park, MN, United StatesComplaint file establishment, Manufacturer, Specification developer6December 14, 2012000api.fda.gov
United States Endoscopy Group, Inc.Mentor, OH, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler3September 7, 2010000api.fda.gov
Boston Scientific Corp., Marina Bay Cust. Fulfillment CenterQuincy, MA, United StatesManufacturer, Manufacturer for export2September 3, 2026000api.fda.gov
Boston Scientific CorporationSaint Paul, MN, United StatesComplaint file establishment, Manufacturer, Manufacturer for export2September 3, 2026000api.fda.gov
Conmed CorporationUtica, NY, United StatesComplaint file establishment, Manufacturer2September 10, 1998000api.fda.gov
Conmed CorporationWestborough, MA, United StatesSpecification developer2September 10, 1998000api.fda.gov
Covidien llcSanta Clara, CA, United StatesSpecification developer2January 18, 2018000api.fda.gov
Endo-Therapeutics, Inc.Clearwater, FL, United StatesManufacturer2May 8, 1980000api.fda.gov
Apyx Medical CorporationClearwater, FL, United StatesManufacturer1January 30, 1995000api.fda.gov
Boston Scientific CorporationSpencer, IN, United StatesManufacturer1March 20, 1981000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer1August 4, 1988000api.fda.gov
Cook IncorporatedSpencer, IN, United StatesManufacturer1August 4, 1988000api.fda.gov
Francis MedicalMaple Grove, MN, United StatesManufacturer1November 26, 2025000api.fda.gov
Hobbs Medical, Inc.Stafford Springs, CT, United StatesContract manufacturer, Manufacturer1August 2, 2010000api.fda.gov
Merit Medical Systems, Inc.South Jordan, UT, United StatesManufacturer1September 7, 2010000api.fda.gov
Medfiniti, IncTampa, FL, United StatesManufacturer1January 14, 2003000api.fda.gov
Stryker EndoscopySan Jose, CA, United StatesManufacturer, Specification developer1August 9, 2004000api.fda.gov
TeleMed SystemsNorthborough, MA, United StatesSpecification developer1December 22, 1999000api.fda.gov
Aptyx - South Glens FallsS Glens Falls, NY, United StatesContract manufacturer0000api.fda.gov
Cirtec MedicalEnfield, CT, United StatesContract manufacturer0000api.fda.gov
Freudenberg Medical, LLCJeffersonville, IN, United StatesContract manufacturer0000api.fda.gov
Grace Manufacturing IncRussellville, AR, United StatesContract manufacturer0000api.fda.gov
Nortech Systems, Inc.Milaca, MN, United StatesContract manufacturer0000api.fda.gov
Smith & Nephew Inc.Mansfield, MA, United StatesManufacturer0000api.fda.gov
Urologix, LLCPlymouth, MN, United StatesManufacturer0000api.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.