danumed Extension Set for Gastrostomy Button

FDA 510(k) K260110 · Danumed Medizintechnik GmbH

Substantially Equivalent

510(k) numberK260110

Submission

Device name
danumed Extension Set for Gastrostomy Button
Applicant
Danumed Medizintechnik GmbH
Regensburg, DE
Received
January 14, 2026
Decision date
September 10, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
PIF – Gastrointestinal Tubes With Enteral Specific Connectors
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

To facilitate enteral specific connections.

Other 510(k)s with product code PIF

510(k)DeviceApplicantDecision
K253715Edi Catheter ENFit 6Fr/48 cm (6893166); Edi Catheter ENFit 6Fr/49cm (6893273); Edi…PIF · Traditional Maquet Critical Care AB08/26/2026SE
K254170Percutaneous Endoscopic Gastrostomy (PEG) KitPIF · Traditional Degania Silicone , Ltd.03/20/2026SE
K242917Enteral Drainage System, Enteral Medicine strawPIF · Traditional HMC Premedical S.p.A.06/18/2025SE
K250481Extension Feeding Set with ENFit™ ConnectorsPIF · Traditional SKY Medical, a.s.04/18/2025SE
K240052Disposable Enteral Feeding SetsPIF · Traditional Beijing L&Z Medical Technology Development Co.…07/03/2024SE
K233034Mobility+ Enteral Feeding System OTCPIF · Traditional Rockfield Medical04/12/2024SE
K230326ENFit to ENFit Extension SetsPIF · Traditional Vesco Medical11/02/2023SE
K232046Kangaroo Skin Level Balloon Gastrostomy Kit, Kangaroo Bolus Feed Set with ENFIT…PIF · Traditional Xeridiem Medical Devices, A Spectrum Plastics…10/06/2023SE
K222773Feeding TubePIF · Traditional Anhui Tiankang Medical Technology Co., Ltd.08/17/2023SE
K223683EnteraLoc FlowPIF · Traditional Vonco Products07/10/2023SE

Questions and answers

When was danumed Extension Set for Gastrostomy Button cleared by the FDA?

danumed Extension Set for Gastrostomy Button (K260110) received a 510(k) decision of Substantially Equivalent on September 10, 2026, 239 days after the submission was received.

What is the product code of K260110?

The FDA product code is PIF – Gastrointestinal Tubes With Enteral Specific Connectors, a Class II (moderate risk) device regulated under 21 CFR 876.5980.