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Data / Medical devices / Cannula, Manipulator/Injector, Uterine / United States

FDA-registered makers of Cannula, Manipulator/Injector, Uterine in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Cannula, Manipulator/Injector, Uterine (product code LKF). 14 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
Cannula, Manipulator/Injector, Uterine
Product code
LKF
Country
United States

Makers of Cannula, Manipulator/Injector, Uterine in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Coopersurgical, Inc.Trumbull, CT, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler13October 28, 2022050api.fda.gov
Medgyn Products, Inc.Westmont, IL, United StatesManufacturer, Repackager or relabeler7January 31, 2013000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer6March 29, 2019000api.fda.gov
Cook IncorporatedSpencer, IN, United StatesManufacturer4March 29, 2019000api.fda.gov
Conmed CorporationUtica, NY, United StatesComplaint file establishment, Manufacturer3February 10, 2015000api.fda.gov
ConMed CorporationGreenwood Village, CO, United StatesSpecification developer3February 10, 2015000api.fda.gov
Femasys Inc.Suwanee, GA, United StatesManufacturer3September 6, 2024000api.fda.gov
Clinical Innovations, LLCMurray, UT, United StatesComplaint file establishment, Manufacturer2May 28, 2014020api.fda.gov
Utah Medical Products, Inc.Midvale, UT, United StatesManufacturer2May 23, 2007000api.fda.gov
Argon Medical Devices Inc.Athens, TX, United StatesContract manufacturer, Manufacturer1June 16, 2000000api.fda.gov
Intuitive Surgical, Inc.Sunnyvale, CA, United StatesSpecification developer1October 9, 2007000api.fda.gov
Kronner Prototypes, Inc.Roseburg, OR, United StatesManufacturer1December 11, 2013000api.fda.gov
Rejoni, IncBedford, MA, United StatesComplaint file establishment, Manufacturer1December 16, 2022000api.fda.gov
Titus Medical LLCRock Hill, SC, United StatesManufacturer1April 30, 2010000api.fda.gov
Allwin Medical Devices, Inc.Anaheim, CA, United StatesManufacturer for export0000api.fda.gov
Argon Medical Devices, Inc.Wheeling, IL, United StatesContract manufacturer0000api.fda.gov
Aptyx - South Glens FallsS Glens Falls, NY, United StatesContract manufacturer0000api.fda.gov
Coloplast Manufacturing Us, LLCMinneapolis, MN, United StatesManufacturer0000api.fda.gov
Elmed, Inc.Glendale Heights, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Lsi Solutions Inc.Victor, NY, United StatesManufacturer0000api.fda.gov
Lone Star Medical ProductsStafford, TX, United StatesContract manufacturer0000api.fda.gov
Phoenix Instruments, Inc.Lisle, IL, United StatesContract manufacturer0000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler0000api.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.