Clinicon Corp.
United StatesFDA applicant, unverified
Clinicon Corp. is a medical device manufacturer, with 30 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 30
Registry facts
- Registries
- FDA GUDID 21
- FDA 510(k) 9
- Device classes
- FDA Class II 30
What Clinicon Corp. makes
Clinicon Corp. manufactures single-use surgical laser accessories, including beam guides and probes designed for compatibility with diode and carbon dioxide laser systems. Products like SureProbe, SureGuide, SureTip, and SureLase are intended for precise tissue interaction during surgical procedures. The portfolio also includes SureScan and SureTouch devices, which appear to support laser targeting and feedback mechanisms.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI registries.
Catalogue
Search and filter all 30 devicesFrequently asked questions
How many devices does Clinicon Corp. have in the registry?
The registry currently lists 30 devices for Clinicon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinicon Corp.'s devices?
Among its 30 most recently registered devices, Clinicon Corp. has devices listed in FDA 510(k) (9 devices) and FDA GUDID (21 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Clinicon Corp.'s devices fall under?
Among its 30 most recently registered devices, the classes recorded for Clinicon Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinicon Corp. in the registry?
The most recently registered devices listed for Clinicon Corp. include SureProbe 4002, SureGuide 4034, SureProbe 4159 and SureScan 3566.