Derma-Lase Co.
Country not established
- Devices
- 5
What Derma-Lase Co. makes
Derma-Lase Co. manufactures medical laser systems, including the DLR-1 Ruby laser and the DLY-1 Multiline laser series. These devices are designed for dermatological applications.
The company is based in the United States, and its portfolio consists of Class II medical devices. These products are listed in the FDA 510(k) regulatory registry.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Multiline; Dly-1 Ref K930793
Regimes: 510(k) Registry: 510(k)Derma-Lase Dla-1 Laser Ref K930975
Regimes: 510(k) Registry: 510(k)Derma-Lase Ruby Laser - Model Dlr-1 Ref K913256
Regimes: 510(k) Registry: 510(k)Multiline; Dly-1 Ref K932156
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Derma-Lase Co. have in the registry?
The registry currently lists 5 devices for Derma-Lase Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Derma-Lase Co.'s devices?
Among its 5 most recently registered devices, Derma-Lase Co. has devices listed in FDA 510(k) (5 devices).
What risk classes do Derma-Lase Co.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Derma-Lase Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Derma-Lase Co. in the registry?
The most recently registered devices listed for Derma-Lase Co. include DLR-1 DERMA-LASE RUBY LASER/DLR-1/DERMA-LASE SYST, MULTILINE; DLY-1, DERMA-LASE DLA-1 LASER and DERMA-LASE RUBY LASER - MODEL DLR-1.