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Data / Medical devices / Device, Percutaneous Retrieval

Device, Percutaneous Retrieval (MMX): 20 FDA-registered makers in 5 countries

20 establishments in 5 countries are registered with the FDA to make Device, Percutaneous Retrieval (product code MMX, Class 2, 21 CFR 870.5150). 13 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 32 510(k) clearances under this code, the latest on February 14, 2025, and lists 1 recall event (1 Class I). FDA data exported November 2, 2026.

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Product code
MMX
Device class
2
Regulation
870.5150
Medical specialty
Cardiovascular

Makers by country

CountryMakers
United States14
Germany2
Costa Rica2
China1
Ireland1

Makers of Device, Percutaneous Retrieval

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Argon Medical Devices Inc.Athens, TX, United StatesContract manufacturer, Manufacturer4January 5, 2021000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer4May 16, 2023011api.fda.gov
Merit Medical Systems, Inc.South Jordan, UT, United StatesManufacturer4January 17, 2020000api.fda.gov
LimFlow Inc.Irvine, CA, United StatesSpecification developer2February 14, 2025000api.fda.gov
Abbott MedicalMinnetonka, MN, United StatesManufacturer1April 1, 2022000api.fda.gov
Abbott MedicalSylmar, CA, United StatesManufacturer1April 1, 2022000api.fda.gov
Bard Peripheral Vascular, Inc.Tempe, AZ, United StatesSpecification developer1February 18, 2016000api.fda.gov
Heraeus Medical Components, LLCSaint Paul, MN, United StatesComplaint file establishment, Specification developer1October 23, 2015000api.fda.gov
Lifetech Scientific (shenzhen) Co,.ltdShenzhen Guangdong, ChinaManufacturer1November 9, 2010000api.fda.gov
Nipro Vascular Innovations Americas, Inc.Sunnyvale, CA, United StatesManufacturer1August 28, 2017000api.fda.gov
Onocor LLCWest Chester, PA, United StatesComplaint file establishment, Specification developer1May 23, 2022000api.fda.gov
Vascular Solutions LLCMaple Grove, MN, United StatesManufacturer1March 8, 2017000api.fda.gov
ev3, Inc.Plymouth, MN, United StatesManufacturer1June 3, 2024000api.fda.gov
C.R. Bard, Inc.Queensbury, NY, United StatesContract manufacturer0000api.fda.gov
Contract Medical International GmbHDRESDEN Saxony, GermanyContract manufacturer0000api.fda.gov
Heraeus Medical Components, SRLGuadalupe Cartago, Costa RicaContract manufacturer0000api.fda.gov
Merit Medical Ireland, LtdGalway Galway(County), IrelandContract manufacturer0000api.fda.gov
Nitinol Devices & Components Costa Rica, S. R. L.El Coyol Alajuela, Costa RicaContract manufacturer0000api.fda.gov
Robling Medical, LLCYoungsville, NC, United StatesContract manufacturer0000api.fda.gov
pfm medical mepro gmbhNonnweiler-Otzenhausen Saarland, GermanyManufacturer0000api.fda.gov

Updated February 14, 2025. 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.