Skip to the page

Data / Medical devices / Catheter, Percutaneous / Costa Rica

FDA-registered makers of Catheter, Percutaneous in Costa Rica: 7 establishments

7 establishments in Costa Rica are registered with the FDA to make Catheter, Percutaneous (product code DQY). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Catheter, Percutaneous
Product code
DQY
Country
Costa Rica

Makers of Catheter, Percutaneous in Costa Rica

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Boston Scientific CorporationLa Aurora Heredia, Costa RicaSpecification developer6January 6, 2017000api.fda.gov
Boston Scientific CorporationCartago, Costa RicaManufacturer2February 1, 2024000api.fda.gov
Boston Scientific CorporationEl Coyol Alajuela, Costa RicaManufacturer2February 1, 2024000api.fda.gov
Abbott VascularEl Coyol Alajuela, Costa RicaExporter to the US, Manufacturer1August 15, 2012000api.fda.gov
Creganna Medical S. R. LSan Rafael Heredia, Costa RicaContract manufacturer0000api.fda.gov
MicroVention Costa Rica S.R.L.. Alajuela, Costa RicaContract manufacturer0000api.fda.gov
Nitinol Devices & Components Costa Rica, S. R. L.El Coyol Alajuela, Costa RicaContract 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.