Dntl Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Dntl Corp. makes
Dntl Corp. manufactures portable radiographic equipment, including mobile X-ray floor stands for on-site imaging and a portable field unit for field deployments. Their dental portfolio includes a portable dental delivery system designed for intraoral imaging and procedures. These devices are intended for use in clinical, field, and dental settings requiring mobility and flexibility.
The company’s products are regulated under the FDA’s 510(k) pathway, with devices classified as Class I and Class II. Their equipment is listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The company is headquartered in the United States.
Catalogue
Mobile X-Ray Floor Stand Ref K912400
510(k) 510(k)Model 2100 Portable Field Unit Ref K911506
510(k) 510(k)Portable Ii Dental Delivery System Ref K883775
510(k) 510(k)
Frequently asked questions
How many devices does Dntl Corp. have in the registry?
The registry currently lists 3 devices for Dntl Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dntl Corp.'s devices?
Among its 3 most recently registered devices, Dntl Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Dntl Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dntl Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dntl Corp. in the registry?
The most recently registered devices listed for Dntl Corp. include MOBILE X-RAY FLOOR STAND, MODEL 2100 PORTABLE FIELD UNIT and PORTABLE II DENTAL DELIVERY SYSTEM.