Vista Ophthalmics, LLC
Country not established
- Devices
- 1
What Vista Ophthalmics, LLC makes
Vista Ophthalmics, LLC manufactures the Vitrectomy Probe, a surgical instrument used in vitreoretinal procedures to remove or manipulate vitreous humor within the eye. The device is designed for precision applications in ophthalmic surgery, aiding in the treatment of conditions such as retinal detachment or diabetic retinopathy.
The Vitrectomy Probe is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Vista Ophthalmics Vitrectomy Probe Ref K220030
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vista Ophthalmics, LLC have in the registry?
The registry currently lists 1 device for Vista Ophthalmics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vista Ophthalmics, LLC's devices?
Among its 1 most recently registered device, Vista Ophthalmics, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Vista Ophthalmics, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vista Ophthalmics, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vista Ophthalmics, LLC in the registry?
The most recently registered devices listed for Vista Ophthalmics, LLC include Vista Ophthalmics Vitrectomy Probe.