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FDA 510(k)

Tigertriever 25 Revascularization Device

K-Number: K253062 · 2026-03-12

ApplicantRapid Medical , Ltd.
Decision Date2026-03-12
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Tigertriever 25 Revascularization Device is a medical device manufactured by Rapid Medical , Ltd.. It received FDA 510(k) clearance on 2026-03-12 under approval number K253062. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Tigertriever 25 Revascularization Device?

Tigertriever 25 Revascularization Device is a medical device that received FDA 510(k) clearance on 2026-03-12. It is manufactured by Rapid Medical , Ltd.. The 510(k) number is K253062.

When was Tigertriever 25 Revascularization Device approved by the FDA?

Tigertriever 25 Revascularization Device received FDA 510(k) clearance on 2026-03-12, under approval number K253062.

What company makes Tigertriever 25 Revascularization Device?

Tigertriever 25 Revascularization Device is manufactured by Rapid Medical , Ltd..

What is the FDA product code for Tigertriever 25 Revascularization Device?

The FDA product code for Tigertriever 25 Revascularization Device is NRY.

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Other Devices by Rapid Medical , Ltd.

K203592Tigertriever and Tigertriever 17 Revascularization Devce K220808Tigertriever 13 Revascularization Device K230429Tigertriever 21 Revascularization Device, Tigertriever 17 Revascularization Device, Tigertriever 13 Revascularization Device DEN230064BraidE Embolization Assist Device K251603Tigertriever 17 Ultra Revascularization Device

Related Devices (Code: NRY)

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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.

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