Home › Device types › FCL
Forceps, Biopsy, Non-Electric
FDA product code FCL · Class 1 · Gastroenterology, Urology
2,367
Registered devices
2,711
Adverse events
11
Recalls
39
510(k) clearances
Devices with this code
BIOPSY GRASPING FORCEPS — SONTEC INSTRUMENTS, INC.BioCeps Biopsy Forceps, Esophageal — ENDO-THERAPEUTICS, INC.Disposable Endoscopic Biopsy Forceps — Ningbo Xinwell Medical Technology Co., Ltd.Disposable Endoscopic Biopsy Forceps — Ningbo Xinwell Medical Technology Co., Ltd.Disposable Endoscopic Biopsy Forceps — Ningbo Xinwell Medical Technology Co., Ltd.Single-Use Biopsy Forceps — Micro-Tech (Nanjing) Co., Ltd.Surgical Direct — Surgical Direct, Inc.MSI Precision Specialty Instruments — Med Saver, Inc.Novo Surgical — NOVO SURGICAL, INC.Radial Jaw 4 — BOSTON SCIENTIFIC CORPORATIONSurtex — SURTEX INSTRUMENTS LTD.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONSurgical Direct — Surgical Direct, Inc.JACKSON BIOPSY FORCEPS — SONTEC INSTRUMENTS, INC.ZKSK — Beijing ZKSK Technology Co.,LtdSingle-Use Biopsy Forceps — Micro-Tech (Nanjing) Co., Ltd.NA — Hangzhou AGS MedTech Co., Ltd.Biopsy Forceps — ENDO-THERAPEUTICS, INC.Single Use Biopsy Forceps — OLYMPUS MEDICAL SYSTEMS CORP.Surgical Direct — Surgical Direct, Inc.Endoch — Endoch IncSingle Use Biopsy Forceps — Zhejiang Chuangxiang Medical Technology Co., LTD.BioCeps Biopsy Forceps — ENDO-THERAPEUTICS, INC.Single Use Biopsy Forceps — Zhejiang Chuangxiang Medical Technology Co., LTD.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-06-30 | Boston Scientific Corporation | Potential for breach in sterile barrier of device packaging. |
| 2026-06-30 | Boston Scientific Corporation | Potential for breach in sterile barrier of device packaging. |
| 2026-06-30 | Boston Scientific Corporation | Potential for breach in sterile barrier of device packaging. |
| 2023-03-24 | Richard Wolf GmbH | Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps c |
| 2023-03-24 | Richard Wolf GmbH | Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps c |
| 2023-03-24 | Richard Wolf GmbH | Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps c |
| 2023-03-24 | Richard Wolf GmbH | Potentially unable to open forceps jaws when the endoscope shaft is bent by about 90 degrees. If, in addition, the proximal forceps shaft is bent, the forceps c |
| 2016-04-15 | Cook Inc. | Increase in reports of polymer degradation of the catheter tip, resulting in tip fracture and/or separation. degradation could include loss of device function, |
| 2010-05-06 | Boston Scientific Corporation | Clevis may detach from the coil preventing the device to open and/or close. Delays in the procedure may result. |
| 2010-05-06 | Boston Scientific Corporation | Clevis may detach from the coil preventing the device to open and/or close. Delays in the procedure may result. |
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.