Tigertriever 25 Revascularization Device
Tigertriever 25 removes thrombus from large intracranial vessels in patients with ischemic stroke within eight hours of symptom onset. Candidates are patients ineligible for thrombolytic…
Tigertriever 25 removes thrombus from large intracranial vessels in patients with ischemic stroke within eight hours of symptom onset. Candidates are patients ineligible for thrombolytic drug therapy or in whom that therapy has failed. It is used by physicians trained in neurointervention and stroke treatment.
A handle slider pulls a nitinol core wire to expand an adjustable braided nitinol mesh. Under fluoroscopy, the physician adjusts the radiopaque mesh to the vessel diameter, allowing it to engage and enclose the clot for retrieval.
Listed Item
The Tigertriever 25 Revascularization Device is a stentriever intended to restore blood flow by removing thrombus from a large intracranial vessel in patients experiencing ischemic stroke
Delivery Compatibility
The device is intended for vessels 2.5 to 6 mm in diameter and requires a microcatheter with an inner diameter of at least 0.025 inch. It is supplied sterile for single use with two insertion loading sheaths.
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) | K253062 |
| Record published | 2026-03-16 |
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 |
|---|---|---|
| TRPP7125 | 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.