Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Taurus Clip

K-Number: K253734 · 2026-03-12

Decision Date2026-03-12
Product CodePKL
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Taurus Clip is a medical device manufactured by Taurus Endoscopy. It received FDA 510(k) clearance on 2026-03-12 under approval number K253734. The device is classified under product code PKL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Taurus Clip?

Taurus Clip is a medical device that received FDA 510(k) clearance on 2026-03-12. It is manufactured by Taurus Endoscopy. The 510(k) number is K253734.

When was Taurus Clip approved by the FDA?

Taurus Clip received FDA 510(k) clearance on 2026-03-12, under approval number K253734.

What company makes Taurus Clip?

Taurus Clip is manufactured by Taurus Endoscopy.

What is the FDA product code for Taurus Clip?

The FDA product code for Taurus Clip is PKL.

Related Devices (Code: PKL)

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.