Angiotech
Country not established
- Devices
- 7
What Angiotech makes
Angiotech manufactures biliary catheters for drainage procedures, including the SKATER BILIARY CATHETER, and tissue-closure devices for surgical applications. These include the Quill PDO Knotless Tissue-Closure Device (Polydioxanone), Quill Polypropylene Knotless Tissue-Closure Device, and the Quill QuadraHelix Tissue-Closure Device. The company also produces the Bio-Seal Lung Biopsy Tract System for sealing post-biopsy sites in the lung.
The company’s devices fall under FDA Class II regulation and are listed via the 510(k) pathway. Products are distributed in the United States, where Angiotech is based.
Catalogue
Skater Biliary Catheter Ref K070610
Regimes: 510(k) Registry: 510(k)Bio-Seal Lung Biopsy Tract System Ref DEN090007
Regimes: De Novo Registry: De Novo- Regimes: 510(k) Registry: 510(k)
Skater Biliary Catheter Ref K073672
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Quill Quadrahelix Tissue-Closure Device Ref K113800
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Angiotech have in the registry?
The registry currently lists 7 devices for Angiotech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angiotech's devices?
Among its 7 most recently registered devices, Angiotech has devices listed in FDA 510(k) (7 devices).
What risk classes do Angiotech's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Angiotech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angiotech in the registry?
The most recently registered devices listed for Angiotech include SKATER BILIARY CATHETER, BIO-SEAL LUNG BIOPSY TRACT SYSTEM, Quill Polypropylene Knotless Tissue-Closure Device, Variable Loop Design and QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE (POLYDIXANONE).