Transdermal Cap, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Transdermal Cap, Inc. makes
Transdermal Cap, Inc. makes laser therapy devices under the LaserCap brand, including models such as the LaserCap LC Pro, LC Elite, LaserCap300, LaserCap224, LaserCap120, and LaserCap80, which are part of the LaserCap Family of Lasers with specified power outputs.
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
LaserCap LC Pro and LC Elite Ref K150613
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
LaserCap Family of Lasers 300, 224, 120 & 80 Ref K203826
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Transdermal Cap, Inc. have in the registry?
The registry currently lists 3 devices for Transdermal Cap, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Transdermal Cap, Inc.'s devices?
Among its 3 most recently registered devices, Transdermal Cap, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Transdermal Cap, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Transdermal Cap, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Transdermal Cap, Inc. in the registry?
The most recently registered devices listed for Transdermal Cap, Inc. include LaserCap LC Pro and LC Elite, LaserCap300, LaserCap224, LaserCap120, LaserCap80 and LaserCap Family of Lasers 300, 224, 120 & 80.