Ddat(UK), Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Ddat(UK), Ltd. makes
Ddat(Uk), Ltd. manufactures the DDAT OMT, a device designed for orthopedic or musculoskeletal applications, likely intended for minimally invasive surgical procedures or orthopedic trauma management.
The DDAT OMT falls under FDA Class II regulation and is listed under the 510(k) clearance pathway. The company is based in the United States.
Catalogue
Ddat Omt Ref K050098
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ddat(Uk), Ltd. have in the registry?
The registry currently lists 1 device for Ddat(Uk), Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ddat(Uk), Ltd.'s devices?
Among its 1 most recently registered device, Ddat(Uk), Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ddat(Uk), Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ddat(Uk), Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ddat(Uk), Ltd. in the registry?
The most recently registered devices listed for Ddat(Uk), Ltd. include DDAT OMT.