FLEXI-PORT™ Power Injectable Implantable Port
K-Number: K260916 · 2026-06-17
Device Summary
Frequently Asked Questions
What is the FLEXI-PORT™ Power Injectable Implantable Port?
FLEXI-PORT™ Power Injectable Implantable Port is a medical device that received FDA 510(k) clearance on 2026-06-17. The listed applicant is Portal Access, Inc.. The 510(k) number is K260916.
When did FLEXI-PORT™ Power Injectable Implantable Port receive FDA 510(k) clearance?
FLEXI-PORT™ Power Injectable Implantable Port received FDA 510(k) clearance on 2026-06-17, under 510(k) number K260916.
Who is the listed applicant for FLEXI-PORT™ Power Injectable Implantable Port?
The FDA 510(k) record lists Portal Access, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXI-PORT™ Power Injectable Implantable Port?
The FDA product code for FLEXI-PORT™ Power Injectable Implantable Port is LJT.
Related Devices (Code: LJT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
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