Imd, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Imd, Inc. makes
Imd, Inc. makes fenestrated nerve block needles, prophyl care solution, and prophyl care paste.
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Fenestrated Nerve Block Needle Ref K113662
Regimes: 510(k) Registry: 510(k)Prophy Care Solution Ref K864215
Regimes: 510(k) Registry: 510(k)Prophy Care Paste Ref K863133
Regimes: 510(k) Registry: 510(k)Prophy Care Solution Ref K865082
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Imd, Inc. have in the registry?
The registry currently lists 4 devices for Imd, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Imd, Inc.'s devices?
Among its 4 most recently registered devices, Imd, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Imd, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Imd, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Imd, Inc. in the registry?
The most recently registered devices listed for Imd, Inc. include FENESTRATED NERVE BLOCK NEEDLE, PROPHY CARE SOLUTION and PROPHY CARE PASTE.