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
| Country | Makers |
|---|---|
| United States | 14 |
| Germany | 2 |
| Costa Rica | 2 |
| China | 1 |
| Ireland | 1 |
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.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Argon Medical Devices Inc. | Athens, TX, United States | Contract manufacturer, Manufacturer | 4 | January 5, 2021 | 0 | 0 | 0 | api.fda.gov |
| Cook Incorporated | Bloomington, IN, United States | Complaint file establishment, Manufacturer | 4 | May 16, 2023 | 0 | 1 | 1 | api.fda.gov |
| Merit Medical Systems, Inc. | South Jordan, UT, United States | Manufacturer | 4 | January 17, 2020 | 0 | 0 | 0 | api.fda.gov |
| LimFlow Inc. | Irvine, CA, United States | Specification developer | 2 | February 14, 2025 | 0 | 0 | 0 | api.fda.gov |
| Abbott Medical | Minnetonka, MN, United States | Manufacturer | 1 | April 1, 2022 | 0 | 0 | 0 | api.fda.gov |
| Abbott Medical | Sylmar, CA, United States | Manufacturer | 1 | April 1, 2022 | 0 | 0 | 0 | api.fda.gov |
| Bard Peripheral Vascular, Inc. | Tempe, AZ, United States | Specification developer | 1 | February 18, 2016 | 0 | 0 | 0 | api.fda.gov |
| Heraeus Medical Components, LLC | Saint Paul, MN, United States | Complaint file establishment, Specification developer | 1 | October 23, 2015 | 0 | 0 | 0 | api.fda.gov |
| Lifetech Scientific (shenzhen) Co,.ltd | Shenzhen Guangdong, China | Manufacturer | 1 | November 9, 2010 | 0 | 0 | 0 | api.fda.gov |
| Nipro Vascular Innovations Americas, Inc. | Sunnyvale, CA, United States | Manufacturer | 1 | August 28, 2017 | 0 | 0 | 0 | api.fda.gov |
| Onocor LLC | West Chester, PA, United States | Complaint file establishment, Specification developer | 1 | May 23, 2022 | 0 | 0 | 0 | api.fda.gov |
| Vascular Solutions LLC | Maple Grove, MN, United States | Manufacturer | 1 | March 8, 2017 | 0 | 0 | 0 | api.fda.gov |
| ev3, Inc. | Plymouth, MN, United States | Manufacturer | 1 | June 3, 2024 | 0 | 0 | 0 | api.fda.gov |
| C.R. Bard, Inc. | Queensbury, NY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Contract Medical International GmbH | DRESDEN Saxony, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Heraeus Medical Components, SRL | Guadalupe Cartago, Costa Rica | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Merit Medical Ireland, Ltd | Galway Galway(County), Ireland | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nitinol Devices & Components Costa Rica, S. R. L. | El Coyol Alajuela, Costa Rica | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Robling Medical, LLC | Youngsville, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| pfm medical mepro gmbh | Nonnweiler-Otzenhausen Saarland, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.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.