Dentimedic
Country not established
- Devices
- 1
What Dentimedic makes
Dentimedic manufactures the Dentimedic Dental Emergency Kit, a Class I medical device designed for immediate dental first aid and emergency response in clinical settings. The kit includes essential tools and supplies for managing acute dental emergencies, such as trauma, bleeding, or acute pain.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class I device, indicating minimal risk. The product is listed in the FDA’s 510(k) database and is intended for use in the United States.
Catalogue
Dentimedic Dental Emergency Kit Ref K861681
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dentimedic have in the registry?
The registry currently lists 1 device for Dentimedic. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dentimedic's devices?
Among its 1 most recently registered device, Dentimedic has devices listed in FDA 510(k) (1 device).
What risk classes do Dentimedic's devices fall under?
Among its 1 most recently registered device, the classes recorded for Dentimedic's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dentimedic in the registry?
The most recently registered devices listed for Dentimedic include DENTIMEDIC DENTAL EMERGENCY KIT.