M.D. Intl., Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
Catalogue
Oxy-Therm Ref K870832
510(k) 510(k)Joy Light Ref K771249
510(k) 510(k)Dmi 250 Series Power Surgery Table Ref K894789
510(k) 510(k)Dmi Series 90 Examination Table Ref K894788
510(k) 510(k)
Frequently asked questions
How many devices does M.D. Intl., Inc. have in the registry?
The registry currently lists 4 devices for M.D. Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list M.D. Intl., Inc.'s devices?
Among its 4 most recently registered devices, M.D. Intl., Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do M.D. Intl., Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for M.D. Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from M.D. Intl., Inc. in the registry?
The most recently registered devices listed for M.D. Intl., Inc. include OXY-THERM, JOY LIGHT, DMI 250 SERIES POWER SURGERY TABLE and DMI SERIES 90 EXAMINATION TABLE.