Tigertriever 17 Ultra Revascularization Device
The Tigertriever 17 Ultra removes clots from large intracranial vessels to restore blood flow in ischaemic stroke within eight hours of symptom onset. It is intended for patients who cannot…
The Tigertriever 17 Ultra removes clots from large intracranial vessels to restore blood flow in ischaemic stroke within eight hours of symptom onset. It is intended for patients who cannot receive thrombolytic drug treatment or for whom that treatment has failed.
A handle slider expands an adjustable nitinol mesh through a core wire inside the shaft. The physician observes the radiopaque mesh under fluoroscopy and adjusts it to the vessel diameter. The mesh engages and surrounds the clot for retrieval.
Listed Item
The Tigertriever 17 Ultra Revascularization Device is a stentriever intended to restore blood flow by removing thrombus from a large intracranial vessel in patients experiencing ischemic stroke
Delivery and Use
Model TRPP7266 is supplied sterile for single use by physicians trained in neurointervention and ischaemic stroke treatment. It requires a microcatheter with an inner diameter of at least 0.017 inch.
Who Else Makes It
Concentrated in Shanghai (3), Jiangsu (2). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Covidien Medical Products (Shanghai) Manufacturing LLC | Shanghai | Shanghai | Contract manufacturer | 8 |
| Sterigenics Shanghai ETO Ltd. | Shanghai | Shanghai | Contract manufacturer | 65 |
| Steris Sterilization Technologies (Suzhou) Ltd | Suzhou | Jiangsu | Contract manufacturer | 44 |
| Suzhou Zenith Vascular Scitech Limited | Suzhou | Jiangsu | Manufacturer | 6 |
| Shanghai Wallaby Medical Technologies Co., Inc. | Shanghai | Shanghai | Contract manufacturer | 5 |
Record
| Listed by | Rapid-Medical Ltd, Israel |
|---|---|
| FDA product code | NRY |
| Device type | Catheter, Thrombus Retriever |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1250 |
| Establishment | Complaint-file establishment, Manufacturer |
| 510(k) | K251603 |
| Record published | 2025-11-17 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: Store in a dry place at room temperature in its designated box |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| TRPP7266 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Penumbra System | Penumbra Inc. | 100 |
| RED 43 | Penumbra Inc. | 18 |
| Solitaire™ X-Pack | Micro Therapeutics, Inc. | 14 |
| ACE | Penumbra Inc. | 14 |
| Raptor Aspiration Catheter | Balt USA, LLC | 13 |
| Cereglide | Cerenovus, Inc. | 13 |
| Solitaire™ | Micro Therapeutics, Inc. | 9 |
| Solitaire™ X | Micro Therapeutics, Inc. | 9 |
| RED 68 | Penumbra Inc. | 9 |
| Riptide™ | Micro Therapeutics, Inc. | 9 |
| Zoom™ Reperfusion Catheter | Imperative Care Inc. | 9 |
| CaptureTM | Micro Therapeutics, Inc. | 8 |
Showing 12 of 80. All products under Catheter, Thrombus Retriever
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K260617 | 2026-08-28 |
| K253062 | 2026-03-12 |
| K251603 | 2025-10-06 |
| K230429 | 2023-04-17 |
| K220808 | 2022-07-25 |
| K203592 | 2021-03-23 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.