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Data / Medical devices / Catheter, Assisted Reproduction / United States

FDA-registered makers of Catheter, Assisted Reproduction in the United States: 6 establishments

6 establishments in the United States are registered with the FDA to make Catheter, Assisted Reproduction (product code MQF). 6 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
Catheter, Assisted Reproduction
Product code
MQF
Country
United States

Makers of Catheter, Assisted Reproduction in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Cook IncorporatedSpencer, IN, United StatesManufacturer10May 17, 2019000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer9May 17, 2019020api.fda.gov
Coopersurgical, Inc.Trumbull, CT, United StatesManufacturer, Specification developer6December 19, 2003000api.fda.gov
Medgyn Products, Inc.Westmont, IL, United StatesManufacturer6November 23, 2015000api.fda.gov
Allwin Medical Devices, Inc.Anaheim, CA, United StatesManufacturer2July 1, 2020000api.fda.gov
Femasys Inc.Suwanee, GA, United StatesManufacturer1September 22, 2023000api.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.