Krupp International, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Krupp International, Inc. makes
Krupp International, Inc. manufactures dental alloys for restorative and prosthetic applications, as well as nuclear medicine data acquisition and information systems for diagnostic imaging.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance pathway. These products are based in the United States.
Catalogue
Dental Alloy Ref K780090
510(k) 510(k)Kandi-Nuclear Med. Data Acqu.&Info. Ref K800835
510(k) 510(k)
Frequently asked questions
How many devices does Krupp International, Inc. have in the registry?
The registry currently lists 2 devices for Krupp International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Krupp International, Inc.'s devices?
Among its 2 most recently registered devices, Krupp International, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Krupp International, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Krupp International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Krupp International, Inc. in the registry?
The most recently registered devices listed for Krupp International, Inc. include DENTAL ALLOY and KANDI-NUCLEAR MED. DATA ACQU.&INFO..