Cavitron Corp.
United StatesFDA applicant, unverified
- Devices
- 32
What Cavitron Corp. makes
Cavitron Corp. manufactures medical devices including an ultrasonic surgical aspirator (CUSA), blood pressure measurement options for sphygmomanometers, phototherapy lamps and meters, patient monitors for respiratory carbon dioxide and CO₂ levels, transport incubators, and dental polishing systems. Their product line also covers oxygen analyzers, electrosurgical tools for dental procedures, and temperature monitoring modules for medical use.
The company’s devices are classified under FDA categories Class I, Class II, and Unclassified (U), with most products subject to 510(k) clearance. These devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Search and filter all 32 devicesFrequently asked questions
How many devices does Cavitron Corp. have in the registry?
The registry currently lists 32 devices for Cavitron Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cavitron Corp.'s devices?
Among its 32 most recently registered devices, Cavitron Corp. has devices listed in FDA 510(k) (32 devices).
What risk classes do Cavitron Corp.'s devices fall under?
Among its 32 most recently registered devices, the classes recorded for Cavitron Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cavitron Corp. in the registry?
The most recently registered devices listed for Cavitron Corp. include ULTRASPHYG BLOOD PRESSURE OPTION, PHOTOTHERAPY/PROCEDURE LAMP, CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5 and TRANSPORT INCUBATOR.