Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account
MMX — Predicate Candidate Screening
32 FDA 510(k) clearances under this product code; the 50 most recent screened below.
96 daysmedian FDA review time
213 days90th percentile
32clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K242776 | LimFlow V-Ceiver | LimFlow, Inc. | 2025-02-14 | 154 | 0 |
| K241259 | Amplatz Goose Neck Snare Kit | Medtronic, Inc. | 2024-06-03 | 28 | 0 |
| K232443 | Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval | Argon Medical Devices, Inc. | 2023-09-07 | 24 | 0 |
| K222254 | Gunther Tulip Vena Cava Filter Retrieval Set | Cook Incorporated | 2023-05-16 | 293 | 0 |
| K222083 | LimFlow V-Ceiver | LimFlow, Inc. | 2022-08-09 | 25 | 0 |
| K212988 | ONO Retrieval Device | Onocor Vascular, LLC | 2022-05-23 | 245 | 0 |
| K213494 | Aveir Retrieval Catheter | ABBOTT MEDICAL | 2022-04-01 | 151 | 0 |
| K200963 | Halo Single-Loop Microsnare Kit | Argon Medical Devices, Inc. | 2021-01-05 | 270 | 0 |
| K200268 | Halo™ Single-Loop Snare Kit | Argon Medical Devices, Inc. | 2020-06-03 | 121 | 0 |
| K193507 | Merit ONE Snare System | Merit Medical Systems, Inc. | 2020-01-17 | 30 | 0 |
| K191758 | Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval | Argon Medical Devices, Inc. | 2019-12-17 | 169 | 0 |
| K181757 | Günther Tulip® Vena Cava Filter Retrieval Set | Cook Incorporated | 2018-11-06 | 127 | 0 |
| K170987 | Captus Vascular Retrieval System | Avantec Vascular Corporation | 2017-08-28 | 147 | 0 |
| K163307 | Expro Elite Snare, Sympro Elite Snare | Vascular Solutions, Inc. | 2017-03-08 | 105 | 0 |
| K160593 | Indy OTW Vascular Retriever | Cook Incorporated | 2016-09-02 | 185 | 0 |
| K152136 | Recovery Cone Removal System | C.R. Bard, Inc. | 2016-02-18 | 202 | 0 |
| K152560 | Bard Snare Retrieval Kit | Neometrics, Inc. | 2015-10-23 | 44 | 0 |
| K151497 | EN Snare Endovascular Snare System | Merit Medical Systems, Inc. | 2015-07-01 | 27 | 0 |
| K142265 | ONE Snare Endovascular Microsnare System | Merit Medical Systems, Inc. | 2014-11-13 | 90 | 0 |
| K133681 | CRUX SNARE FILTER RETRIEVAL SET | Volcano Corporation | 2014-01-30 | 59 | 0 |
| K122088 | MERIT ONE SNARE SYSTEM | Merit Medical Systems, Inc. | 2012-12-05 | 142 | 0 |
| K112185 | FOURSNARE VASCULAR RETRIEVAL SNARE | Cook, Inc. | 2011-11-02 | 96 | 1 |
| K102484 | SEQURE SNARE SYSTEM | Lifetech Scientific (Shenzhen) Co., Ltd. | 2010-11-09 | 71 | 0 |
| K092343 | EN SNARE ENDOVASCULAR SNARE SYSTEM | Merit Medical Systems, Inc. | 2009-08-07 | 3 | 0 |
| K091563 | RECRUIT MICROCATHETER | Reverse Medical Corporation | 2009-07-30 | 63 | 0 |
| K071457 | MODIFICATION TO RADIUS SNARE | Radius Medical Technologies, Inc. | 2007-09-25 | 123 | 0 |
| K050926 | TEXAN LONGHORN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX301200 | Idev Technologies, Inc. | 2005-05-09 | 26 | 0 |
| K033188 | TEXAN FOREIGN BODY RETRIEVAL DEVICE, MODEL TX30060050 | Idev Technologies, Inc. | 2003-11-19 | 49 | 0 |
| K022201 | RADIUS MICRO SNARE | Radius Medical Technologies, Inc. | 2003-02-03 | 213 | 0 |
| K021441 | RADIUS SNARE | Radius Medical Technologies, Inc. | 2002-06-14 | 39 | 0 |
| K021606 | EN-SNARE ENDOVASCULAR SNARE AND CATHETER | Medical Device Technologies, Inc. | 2002-05-31 | 15 | 0 |
| K014109 | IN-TIME RETRIEVAL DEVICE | Boston Scientific, Target | 2002-03-12 | 88 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda