Nissel, Ltd.
Country not established
- Devices
- 2
What Nissel, Ltd. makes
Nissel, Ltd. manufactures ophthalmic devices, including an artificial eye implant and various soft (hydrophilic) contact lenses designed for extended or daily wear, such as the S-38 Polymacon lens and the Esstech PS & SV Polymacon lenses.
The company’s products are regulated under FDA Class I and Class II classifications, with relevant devices listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
The Nissel Artificial Eye Ref K923167
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nissel, Ltd. have in the registry?
The registry currently lists 2 devices for Nissel, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nissel, Ltd.'s devices?
Among its 2 most recently registered devices, Nissel, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nissel, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nissel, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nissel, Ltd. in the registry?
The most recently registered devices listed for Nissel, Ltd. include THE NISSEL ARTIFICIAL EYE and S-38 (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS, THE ESSTECH PS & SV (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS.