Texas Applied Biomedical Services
Country not established
- Devices
- 2
What Texas Applied Biomedical Services makes
Texas Applied Biomedical Services manufactures the Trilumina Therapeutic Laser System, a medical device designed for therapeutic laser treatments. This system is intended for clinical applications requiring controlled laser energy delivery to tissues, such as wound healing, pain management, or soft tissue repair.
The Trilumina Therapeutic Laser System is classified as a Class II device under FDA regulations and has been authorised through the 510(k) clearance process. The company operates within the United States, adhering to domestic regulatory standards for medical devices.
Catalogue
Lumix 3 Plus And Lumix 3 Ultra System Ref K132016
Regimes: 510(k) Registry: 510(k)Trilumina Therapeutic Laser System Ref K023935
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Texas Applied Biomedical Services have in the registry?
The registry currently lists 2 devices for Texas Applied Biomedical Services. Devices recorded under merged duplicate company entries are counted once.
Which registries list Texas Applied Biomedical Services's devices?
Among its 2 most recently registered devices, Texas Applied Biomedical Services has devices listed in FDA 510(k) (2 devices).
What risk classes do Texas Applied Biomedical Services's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Texas Applied Biomedical Services's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Texas Applied Biomedical Services in the registry?
The most recently registered devices listed for Texas Applied Biomedical Services include LUMIX 3 PLUS AND LUMIX 3 ULTRA SYSTEM and TRILUMINA THERAPEUTIC LASER SYSTEM.