Tri-Star Ophthalmic
Country not established
- Devices
- 2
What Tri-Star Ophthalmic makes
Tri-Star Ophthalmic manufactures disposable phacoemulsification systems, including the TRI-STAR Universal I/A Phaco Pak and phaco tips designed for cataract surgery procedures. These products are intended for use with phacoemulsification machines to remove clouded lenses from the eye.
The company’s portfolio is classified under FDA Class II devices and is listed in the FDA’s 510(k) registry. The devices are regulated under the US jurisdiction.
Catalogue
Tri-Star Universal I/A Phaco Pak Ref K953359
Regimes: 510(k) Registry: 510(k)Phaco Tip Ref K914229
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tri-Star Ophthalmic have in the registry?
The registry currently lists 2 devices for Tri-Star Ophthalmic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tri-Star Ophthalmic's devices?
Among its 2 most recently registered devices, Tri-Star Ophthalmic has devices listed in FDA 510(k) (2 devices).
What risk classes do Tri-Star Ophthalmic's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tri-Star Ophthalmic's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tri-Star Ophthalmic in the registry?
The most recently registered devices listed for Tri-Star Ophthalmic include TRI-STAR UNIVERSAL I/A PHACO PAK and PHACO TIP.