Zeiss
Country not established
- Devices
- 2
What Zeiss makes
ZEISS manufactures bipolar coagulation forceps and sunglass lenses.
The company is based in the US, and its portfolio includes Class I and Class II devices that are listed in the FDA 510(k) registry.
Catalogue
Select Bipolar Coagulation Forceps Ref K821263
510(k) 510(k)Sunglass Lenses Ref K822573
510(k) 510(k)
Frequently asked questions
How many devices does ZEISS have in the registry?
The registry currently lists 2 devices for ZEISS. Devices recorded under merged duplicate company entries are counted once.
Which registries list ZEISS's devices?
Among its 2 most recently registered devices, ZEISS has devices listed in FDA 510(k) (2 devices).
What risk classes do ZEISS's devices fall under?
Among its 2 most recently registered devices, the classes recorded for ZEISS's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from ZEISS in the registry?
The most recently registered devices listed for ZEISS include SELECT BIPOLAR COAGULATION FORCEPS and SUNGLASS LENSES.