Naimco, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Naimco, Inc. makes
Naimco, Inc. manufactures iontophoresis drug delivery electrodes (models 201-400, 201-401, 201-402, 201-403, and 201-405) and EZ-STIK electrodes for transdermal medication application, as well as the Sonic-Stim device for ultrasound-based stimulation.
These products are classified as Class II medical devices in the US and are listed under FDA 510(k) registrations. The company is based in the United States.
Catalogue
Naimco, Inc., Iontophoresis Drug Delivery Electrodes, Models 201-400, 201-401, 201-402, 201-403 And 201-405 Ref K040495
Regimes: 510(k) Registry: 510(k)Ez-Stik Electrodes Ref K050469
Regimes: 510(k) Registry: 510(k)Sonic-Stim Ref K063135
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Naimco, Inc. have in the registry?
The registry currently lists 3 devices for Naimco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Naimco, Inc.'s devices?
Among its 3 most recently registered devices, Naimco, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Naimco, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Naimco, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Naimco, Inc. in the registry?
The most recently registered devices listed for Naimco, Inc. include NAIMCO, INC., IONTOPHORESIS DRUG DELIVERY ELECTRODES, MODELS 201-400, 201-401, 201-402, 201-403 AND 201-405, EZ-STIK ELECTRODES and SONIC-STIM.