Home › Device types › FDI
Snare, Flexible
FDA product code FDI · Class 2 · Gastroenterology, Urology
557
Registered devices
4,640
Adverse events
18
Recalls
63
510(k) clearances
Devices with this code
Multiple Loop Polypectomy Snare — Avanos Medical, Inc.ClearGrasp Snare — FINEMEDIX CO.,LTD.Rotatable Snare — BOSTON SCIENTIFIC CORPORATIONNA — Hangzhou AGS MedTech Co., Ltd.Non-Rotatable Snares — Zhejiang Chuangxiang Medical Technology Co., LTD.ClearGrasp Snare — FINEMEDIX CO.,LTD.PROFILE — BOSTON SCIENTIFIC CORPORATIONNA — Hangzhou AGS MedTech Co., Ltd.CAPTIVATOR — BOSTON SCIENTIFIC CORPORATIONSnare Wire — OLYMPUS MEDICAL SYSTEMS CORP.NA — Hangzhou AGS MedTech Co., Ltd.Rotator — US EndoscopyELECTROSURGICAL SNARE — OLYMPUS MEDICAL SYSTEMS CORP.Halyard — Avanos Medical, Inc.Roth Net Platinum — US EndoscopyEdgeHog(TM) Polypectomy Snare — Micro-Tech (Nanjing) Co., Ltd.NA — Hangzhou AGS MedTech Co., Ltd.FTRD System Set — Ovesco Endoscopy AGNon-Rotatable Snares — Zhejiang Chuangxiang Medical Technology Co., LTD.Non-Rotatable Snares — Zhejiang Chuangxiang Medical Technology Co., LTD.ClearGrasp Snare — FINEMEDIX CO.,LTD.ClearGrasp Snare — FINEMEDIX CO.,LTD.ZKSK — Beijing ZKSK Technology Co.,LtdNon-Rotatable Snares — Zhejiang Chuangxiang Medical Technology Co., LTD.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-10-06 | Olympus Corporation of the Americas | Sterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf car |
| 2025-10-06 | Olympus Corporation of the Americas | Sterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf car |
| 2021-01-19 | Boston Scientific Corporation | Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient. |
| 2021-01-19 | Boston Scientific Corporation | Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient. |
| 2021-01-19 | Boston Scientific Corporation | Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient. |
| 2020-07-06 | Boston Scientific Corporation | BSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended wou |
| 2020-07-06 | Boston Scientific Corporation | BSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended wou |
| 2020-07-06 | Boston Scientific Corporation | BSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended wou |
| 2020-07-06 | Boston Scientific Corporation | BSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended wou |
| 2020-07-06 | Boston Scientific Corporation | BSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended wou |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
