Incisive Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Incisive Technologies, Inc. makes
Incisive Technologies, Inc. manufactures dental laser systems, including the PulseJet Dental Laser System and standalone Dental Laser Fiber System for soft tissue procedures. Their PulseMaster S Series provides adjustable laser parameters for precision applications in dentistry.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
Pulsejet Dental Laser System Ref K942217
Regimes: 510(k) Registry: 510(k)Dental Laser Fiber System Ref K945143
Regimes: 510(k) Registry: 510(k)Pulsemaster S Series Ref K943693
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Incisive Technologies, Inc. have in the registry?
The registry currently lists 5 devices for Incisive Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Incisive Technologies, Inc.'s devices?
Among its 5 most recently registered devices, Incisive Technologies, Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Incisive Technologies, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Incisive Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Incisive Technologies, Inc. in the registry?
The most recently registered devices listed for Incisive Technologies, Inc. include BlueCheck BN01AUS, BlueCheck BN01BUS, PULSEJET DENTAL LASER SYSTEM and DENTAL LASER FIBER SYSTEM.