Clinical Technology Corp.
United StatesFDA applicant, unverified
- Devices
- 12
What Clinical Technology Corp. makes
Clinical Technology Corp. makes electrosurgical generators and accessories, ultrasonic surgical aspirators and systems, disposable arthroscopy cannula sets, hemoglobin test kits for separating hemoglobin and screening sickle cell hemoglobin, urinary bladder temperature sensors, and related surgical and diagnostic devices such as Steri-Grip and Tek-Lube.
The company's devices are classified as Class I, Class II, and unclassified (U) and are listed in the FDA 510(k) registry. Clinical Technology Corp. is based in the United States.
Catalogue
Search and filter all 12 devicesFrequently asked questions
How many devices does Clinical Technology Corp. have in the registry?
The registry currently lists 12 devices for Clinical Technology Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinical Technology Corp.'s devices?
Among its 12 most recently registered devices, Clinical Technology Corp. has devices listed in FDA 510(k) (12 devices).
What risk classes do Clinical Technology Corp.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for Clinical Technology Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinical Technology Corp. in the registry?
The most recently registered devices listed for Clinical Technology Corp. include BIOSIGN, GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN, BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000 and ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES.