Barbed PDO Suture
K-Number: K252171 · 2026-06-12
Device Summary
Frequently Asked Questions
What is the Barbed PDO Suture?
Barbed PDO Suture is a medical device that received FDA 510(k) clearance on 2026-06-12. The listed applicant is Sutura Medical Technology, Inc.. The 510(k) number is K252171.
When did Barbed PDO Suture receive FDA 510(k) clearance?
Barbed PDO Suture received FDA 510(k) clearance on 2026-06-12, under 510(k) number K252171.
Who is the listed applicant for Barbed PDO Suture?
The FDA 510(k) record lists Sutura Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Barbed PDO Suture?
The FDA product code for Barbed PDO Suture is NEW.
Related Devices (Code: NEW)
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.