Laser Media
Country not established
- Devices
- 13
What Laser Media makes
Laser Media manufactures ND:YAG laser systems for medical use, including reusable and single-use models designed for pulmonary, gastrointestinal, urological, and gynecological applications. Their portfolio includes both medical laser systems and fiber delivery systems, such as the FiberLase II and FiberLase 100 series, as well as disposable fiber optics for laser treatment. These devices are intended for procedures like menorrhagia treatment, bronchoscopy, and endoscopic interventions.
The company’s products are regulated under FDA Class II and Class III designations, with authorisations recorded via 510(k) clearances and PMA submissions. Their devices are listed in the FDA’s regulatory databases, and the company is based in the United States.
Catalogue
Search and filter all 13 devicesFrequently asked questions
How many devices does Laser Media have in the registry?
The registry currently lists 13 devices for Laser Media. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laser Media's devices?
Among its 13 most recently registered devices, Laser Media has devices listed in FDA 510(k) (12 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Laser Media's devices fall under?
Among its 13 most recently registered devices, the classes recorded for Laser Media's devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Laser Media in the registry?
The most recently registered devices listed for Laser Media include FIBERLASE II ND:YAG LASER FOR PULMONARY USE, ND:YAG LASER SINGLE USE FIBER DELIVERY SYSTEM, FIBERLASE 100 ND: YAG MEDICAL LASER SYSTEM and SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAG.