Gastroenterology & Urology devices: recent FDA 510(k) clearances
27 gastroenterology & Urology devices: recent FDA 510(k) clearances are listed from U.S. FDA openFDA, dated 2026-09-11 to 2026-10-23; the most frequent is Ovesco Endoscopy AG with 2. Data last updated 2026-11-04; each record links to its official source and a full report.
Data as of · Compiled by Zalwin from U.S. FDA openFDA
Includes: Record, Specialty, Date, Review days, Recall class, official source URL and score · Card, Apple Pay, Google Pay or Link via Stripe
27 records from U.S. FDA openFDA, dated 2026-09-11 to 2026-10-23. Most frequent: Ovesco Endoscopy AG (2). Each record links to a full report and the official source.
Last updated 2026-11-04. Source: U.S. FDA openFDA.
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- Ovesco Endoscopy AG (2)
- CapsoVision, Inc. (1)
- Canyon Medical, Inc. (1)
- Poly Medicure Limited (1)
- Vein 360 (1)
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What are the top gastroenterology & Urology devices: recent FDA 510(k) clearances right now?
Browse 12 more matching record reports
- MEDIVATORS ADVANTAGE NXT Automated Endoscope Reprocessor (K261791): 510(k) cleared for Steris
- Hemostatic Clip (K261741): 510(k) cleared for Anrei Medical (Hz) Co., Ltd.
- danumed StomaMeter (K262038): 510(k) cleared for Danumed Medizintechnik GmbH
- BTL-299-F (K262353): 510(k) cleared for BTL Industries, Inc.
- Liquick X-treme, Liquick X-treme Plus (K261418): 510(k) cleared for Teleflex Medical
- KARL STORZ TIPCAM1 Rubina (K262547): 510(k) cleared for KALR STORZ SE & Co. KG
- Protégé EverFlex Self-expanding Peripheral Stent System (K262913): 510(k) cleared for Medtronic, Inc.
- Pathfinder Endoscope Overtube (K262262): 510(k) cleared for Neptune Medical, Inc.
- X°Port Heart Preservation System (K261913): 510(k) cleared for Traferox Technologies, Inc.
- Ambu® aScope Gastro; Ambu® aScope Gastro Large (K261400): 510(k) cleared for Ambu A/S
- CVAC® Aspiration System (K261447): 510(k) cleared for Calyxo, Inc.
- CuratOR EX2742 (K262397): 510(k) cleared for Eizo Corporation
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510(k) clearances (414) Class II device recalls (320) Class I device recalls (19) Class III device recalls (11)
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Radiology (56) Orthopedic (53) Cardiovascular (52) General & Plastic Surgery (44) Dental (32) Gastroenterology & Urology (27) Neurology (23) Microbiology (21) Clinical Chemistry (15) General Hospital (14) Anesthesiology (12) Obstetrics & Gynecology (9) Ophthalmic (7)
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Radiology devices: recent FDA 510(k) clearances (56) Orthopedic devices: recent FDA 510(k) clearances (53) Cardiovascular devices: recent FDA 510(k) clearances (52) General & Plastic Surgery devices: recent FDA 510(k) clearances (44) Dental devices: recent FDA 510(k) clearances (32) Neurology devices: recent FDA 510(k) clearances (23) Microbiology devices: recent FDA 510(k) clearances (21) Clinical Chemistry devices: recent FDA 510(k) clearances (15) General Hospital devices: recent FDA 510(k) clearances (14) Anesthesiology devices: recent FDA 510(k) clearances (12) Obstetrics & Gynecology devices: recent FDA 510(k) clearances (9) Ophthalmic devices: recent FDA 510(k) clearances (7)
Frequently asked questions
How many gastroenterology & Urology devices: recent FDA 510(k) clearances are listed?
27 records from U.S. FDA openFDA, last refreshed automatically. The most recent is dated 2026-10-23.
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Source: U.S. FDA openFDA. Informational only. RSS feed of new records
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