Minnesota Laser Corp.
United StatesFDA applicant, unverified
- Devices
- 12
What Minnesota Laser Corp. makes
Minnesota Laser Corp. manufactures surgical laser systems, including carbon dioxide (CO₂) and neodymium-doped yttrium aluminium garnet (Nd:YAG) lasers. Their devices are designed for dermatology, gastroenterology, urology, pulmonary procedures, gynecology, general and plastic surgery, neurology, and otorhinolaryngology (ear, nose, and throat) microsurgery. The systems are intended for precision tissue ablation, coagulation, and vaporisation in clinical settings.
The company’s portfolio consists of Class II medical devices, regulated under the FDA’s 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 12 devicesFrequently asked questions
How many devices does Minnesota Laser Corp. have in the registry?
The registry currently lists 12 devices for Minnesota Laser Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Minnesota Laser Corp.'s devices?
Among its 12 most recently registered devices, Minnesota Laser Corp. has devices listed in FDA 510(k) (12 devices).
What risk classes do Minnesota Laser Corp.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for Minnesota Laser Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Minnesota Laser Corp. in the registry?
The most recently registered devices listed for Minnesota Laser Corp. include PORTALASE 200 CARBON SURGICAL LASER SYSTEM, PORTALASE 200 CARBON DIOXIDE SURG LASER DERMATOLOG, ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA. and ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI..