Smartmissimo Technologies Pte, Ltd.
SingaporeFDA applicant, unverified
- Devices
- 5
What Smartmissimo Technologies Pte, Ltd. makes
Smartmissimo Technologies Pte, Ltd. makes the PowerDot(R) PD-01 Muscle Stimulator and related models including the PD-01MT, PD-01MT2, and PD-01M, which are neuromuscular electrical stimulation devices designed for muscle conditioning and recovery, and are used with the PowerDot(R) Mobile Application.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
PowerDot PD-01MT Ref K181759
Regimes: 510(k) Registry: 510(k)PowerDot PD-01MT2 Muscle Stimulator Ref K210269
Regimes: 510(k) Registry: 510(k)PowerDot PD-01M Ref K172876
Regimes: 510(k) Registry: 510(k)PowerDot PD-01MT2 Muscle Stimulator Ref K210938
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Smartmissimo Technologies Pte, Ltd. have in the registry?
The registry currently lists 5 devices for Smartmissimo Technologies Pte, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Smartmissimo Technologies Pte, Ltd.'s devices?
Among its 5 most recently registered devices, Smartmissimo Technologies Pte, Ltd. has devices listed in FDA 510(k) (5 devices).
What risk classes do Smartmissimo Technologies Pte, Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Smartmissimo Technologies Pte, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Smartmissimo Technologies Pte, Ltd. in the registry?
The most recently registered devices listed for Smartmissimo Technologies Pte, Ltd. include PowerDot(R) PD-01 Muscle Stimulator (with PowerDot(R) Mobile Application), PowerDot PD-01MT, PowerDot PD-01MT2 Muscle Stimulator and PowerDot PD-01M.