Staar Sugical
Country not established
- Devices
- 2
What Staar Sugical makes
Staar Surgical manufactures the Disposable MicroStaar Injector, a single-use device for ocular procedures, and StaarVisc™ Sodium Hyaluronate, a sterile ophthalmic viscosurgical device used to maintain chamber depth during cataract surgery.
These products are classified as Class I medical devices and are authorised via FDA 510(k) and PMA pathways. The company is headquartered in the United States.
Catalogue
Disposable Microstaar Injector Ref K940593
Regimes: 510(k) Registry: 510(k)Staarvisc Tm Sodium Hyaluronate Ref P960033
Regimes: PMA, withdrawn Registry: PMA
Frequently asked questions
How many devices does Staar Sugical have in the registry?
The registry currently lists 2 devices for Staar Sugical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Staar Sugical's devices?
Among its 2 most recently registered devices, Staar Sugical has devices listed in FDA 510(k) (1 device) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Staar Sugical's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Staar Sugical's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Staar Sugical in the registry?
The most recently registered devices listed for Staar Sugical include DISPOSABLE MICROSTAAR INJECTOR and STAARVISC TM SODIUM HYALURONATE.