Ronvig Dental Mfg. A/S
DenmarkFDA applicant, unverified FDA FEI 3002808025
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Ronvig Dental Mfg. A/S makes
Ronvig Dental Mfg. A/S manufactures the SEE-IT caries detector, a device designed to identify dental caries (tooth decay) through visual inspection technology.
The SEE-IT caries detector is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
See-It Caries Detector Ref K060330
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3002808025
- Address
- GL. VEJLEVEJ 59, DAUGAARD Midtjylland
Frequently asked questions
How many devices does Ronvig Dental Mfg. A/S have in the registry?
The registry currently lists 1 device for Ronvig Dental Mfg. A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ronvig Dental Mfg. A/S's devices?
Among its 1 most recently registered device, Ronvig Dental Mfg. A/S has devices listed in FDA 510(k) (1 device).
What risk classes do Ronvig Dental Mfg. A/S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ronvig Dental Mfg. A/S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ronvig Dental Mfg. A/S in the registry?
The most recently registered devices listed for Ronvig Dental Mfg. A/S include SEE-IT CARIES DETECTOR.