Tissue Medical Lasers, Inc.
Country not established
- Devices
- 1
What Tissue Medical Lasers, Inc. makes
Tissue Medical Lasers, Inc. manufactures the SPECTRA-VRM Q-switched Nd:YAG laser system, designed for dermatological and medical laser treatments. This device is used for procedures such as tattoo removal, pigmented lesion treatment, and vascular lesion management.
The SPECTRA-VRM system is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tissue Medical Lasers, Inc. have in the registry?
The registry currently lists 1 device for Tissue Medical Lasers, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tissue Medical Lasers, Inc.'s devices?
Among its 1 most recently registered device, Tissue Medical Lasers, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Tissue Medical Lasers, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tissue Medical Lasers, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tissue Medical Lasers, Inc. in the registry?
The most recently registered devices listed for Tissue Medical Lasers, Inc. include SPECTRA-VRM Q-SWITCHED ND:YAG LASER SYSTEM, SPECTRA-VRM.