Spectrum Medical Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Spectrum Medical Technologies, Inc. makes
Spectrum Medical Technologies, Inc. manufactures ruby laser systems designed for medical hair removal and skin treatments, including the EPILASER in normal mode and the RD-1200 series laser systems.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Epilaser Normal Mode Ruby Laser Ref K963947
Regimes: 510(k) Registry: 510(k)Model Rd-1200 Ruby Laser System Ref K910422
Regimes: 510(k) Registry: 510(k)Rd-1200H Normal Mode Ruby Laser System Ref K955612
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spectrum Medical Technologies, Inc. have in the registry?
The registry currently lists 3 devices for Spectrum Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spectrum Medical Technologies, Inc.'s devices?
Among its 3 most recently registered devices, Spectrum Medical Technologies, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Spectrum Medical Technologies, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Spectrum Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spectrum Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Spectrum Medical Technologies, Inc. include EPILASER NORMAL MODE RUBY LASER, MODEL RD-1200 RUBY LASER SYSTEM and RD-1200H NORMAL MODE RUBY LASER SYSTEM.