Titan Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Titan Medical, Inc. makes
Titan Medical, Inc. manufactures vascular catheter placement kits and percutaneous port access devices, including the VASCATH VASCULAR CATHETER PLACEMENT KIT, SURECATH - ITP II PERCUTANEOUS PORT ACCESS DEVICE, and SURECATH-ITP PERCUTANEOUS ACCESS KIT.
The company's products are Class II devices listed in the FDA 510(k) registry, and Titan Medical is based in the US.
Catalogue
Vascath Vascular Catheter Placement Kit Ref K870542
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Surecath-Itp Percutaneous Access Kit Ref K872149
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Titan Medical, Inc. have in the registry?
The registry currently lists 3 devices for Titan Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Titan Medical, Inc.'s devices?
Among its 3 most recently registered devices, Titan Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Titan Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Titan Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Titan Medical, Inc. in the registry?
The most recently registered devices listed for Titan Medical, Inc. include VASCATH VASCULAR CATHETER PLACEMENT KIT, SURECATH - ITP II PERCUTANEOUS PORT ACCESS DEVICE and SURECATH-ITP PERCUTANEOUS ACCESS KIT.