Karl Storz Imaging, Inc.
Country not established FDA establishment FEI 2027009
- Devices
- 10
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
Karl Storz Direct Coupled Camera Head Ref K973252
510(k) 510(k)- 510(k) 510(k)
Karl Storz 3D Video System Ref K001362
510(k) 510(k)- 510(k) 510(k)
- 510(k) 510(k)
Karl Storz Autoclavable Camera Head Ref K994090
510(k) 510(k)- 510(k) 510(k)
- 510(k) 510(k)
Company details
- FDA FEI number
- 2027009
- Address
- 1 S Los Carneros Rd, Goleta, CA, 93117
Frequently asked questions
How many devices does KARL STORZ IMAGING, INC. have in the registry?
The registry currently lists 10 devices for KARL STORZ IMAGING, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list KARL STORZ IMAGING, INC.'s devices?
Among its 10 most recently registered devices, KARL STORZ IMAGING, INC. has devices listed in FDA 510(k) (10 devices).
What risk classes do KARL STORZ IMAGING, INC.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for KARL STORZ IMAGING, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from KARL STORZ IMAGING, INC. in the registry?
The most recently registered devices listed for KARL STORZ IMAGING, INC. include KARL STORZ ENDOVISION DIGIVIDEO (DIGITAL IMAGE PROCESSOR) ACCESSORY FOR COLOR TELEVISION CAMERA USED IN ENDOSCOPIC PROCS, KARL STORZ ENDOVISION XL ENDOSCOPIC CAMERA SYSTEM, KARL STORZ DIRECT COUPLED CAMERA HEAD and OPTRONICS EPIC COLOR TELEVISION CAMERA SYSTEM (S97340).