Liquick X-treme, Liquick X-treme Plus
K-Number: K261418 · 2026-09-23
Device Summary
Frequently Asked Questions
What is the Liquick X-treme, Liquick X-treme Plus?
Liquick X-treme, Liquick X-treme Plus is a medical device that received FDA 510(k) clearance on 2026-09-23. The listed applicant is Teleflex Medical. The 510(k) number is K261418.
When did Liquick X-treme, Liquick X-treme Plus receive FDA 510(k) clearance?
Liquick X-treme, Liquick X-treme Plus received FDA 510(k) clearance on 2026-09-23, under 510(k) number K261418.
Who is the listed applicant for Liquick X-treme, Liquick X-treme Plus?
The FDA 510(k) record lists Teleflex Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Liquick X-treme, Liquick X-treme Plus?
The FDA product code for Liquick X-treme, Liquick X-treme Plus is EZD.
Other records listing Teleflex Medical as applicant
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.
Related Devices (Code: EZD)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.