Atlas FDA

Tigertriever 25 Revascularization Device

FDA 510(k) clearance K253062 · decided 2026-03-12

Clearance details

K-number
K253062
Device name
Tigertriever 25 Revascularization Device
Applicant
Rapid Medical Ltd.
Decision
Substantially Equivalent
Date received
2025-09-22
Decision date
2026-03-12
Days to decision
171 days
Clearance type
Traditional
Product code
NRY
Device class
2
Regulation number
870.1250
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Yokneam, IL
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Socrates Aspiration System (Socrates 70 Aspiration Catheter) (K260002)Scientia Vascular, Inc.2026-07-16
Penumbra System (Thunderbolt Aspiration Tubing) (K250690)Penumbra, Inc.2026-06-10
Zenith Aspiration Catheter; Disposable Aspiration Tubing Set (K252707)Suzhou Zenith Vascular SciTech Limited2026-05-20
Lynx Aspiration Catheter System (K254276)Q’Apel Medical, Inc.2026-05-07
Millipede System (K253590)Perfuze, Ltd.2026-03-16
Esperance pHLO Aspiration System (K251357)Phenox, Ltd.2026-01-15
NeVasc Aspiration System (K251006)Vesalio, Inc.2025-11-10
Zoom System (Zoom 4S Catheter) (K252046)Imperative Care, Inc.2025-10-30
Tigertriever 17 Ultra Revascularization Device (K251603)Rapid Medical Ltd.2025-10-06
EMBOTRAP III Revascularization Device (K251789)Neuravi Limited2025-09-25
Millipede70 Aspiration Catheter; Perfuze Aspiration Tube Set (K252392)Perfuze, Ltd.2025-08-29
CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set (K251828)Cerenovus, Inc.2025-08-22

Recalls involving this device

No recalls on record reference this clearance.