Dicon, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Dicon, Inc. makes
Dicon, Inc. manufactures automated ophthalmic diagnostic devices, including the Auto Perimeter 3000 and 2000 series for visual field testing, as well as the Automatic Objective Refractor 2000 for measuring refractive error without patient input.
These devices are classified as Class I under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Auto Periometer 3000 Ref K822580
Regimes: 510(k) Registry: 510(k)Automatic Objective Refractor 2000 Ref K820877
Regimes: 510(k) Registry: 510(k)Dicon Auto Perimeter 200 Ref K811346
Regimes: 510(k) Registry: 510(k)Dicon Auto Perimeter 2000 Ref K811347
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dicon, Inc. have in the registry?
The registry currently lists 4 devices for Dicon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dicon, Inc.'s devices?
Among its 4 most recently registered devices, Dicon, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Dicon, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Dicon, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dicon, Inc. in the registry?
The most recently registered devices listed for Dicon, Inc. include AUTO PERIOMETER 3000, AUTOMATIC OBJECTIVE REFRACTOR 2000, DICON AUTO PERIMETER 200 and DICON AUTO PERIMETER 2000.