Data / Medical devices / Device, Percutaneous Retrieval / United States
FDA-registered makers of Device, Percutaneous Retrieval in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Device, Percutaneous Retrieval (product code MMX). 12 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Device, Percutaneous Retrieval
- Product code
- MMX
- Country
- United States
Makers of Device, Percutaneous Retrieval in the United States
| 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 |
| 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 | |
| Robling Medical, LLC | Youngsville, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.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.