Matelaser, Inc.
United StatesFDA applicant, unverified FDA FEI 3043840133
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Matelaser, Inc. makes
Matelaser, Inc. manufactures medical laser therapy systems, including the MateLaser Medical Laser Therapy Systems (ML-HIL-30, ML-HIL-60) and the MateLaser Medical Diode Laser Systems (ML-DLS-30).
The company's devices are classified as Class II and are listed in the FDA 510(k) registry. Matelaser, Inc. is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3043840133
- Address
- 3257 NW 7TH AVE CIR, Miami, FL 33127, Miami, FL, 33127
Frequently asked questions
How many devices does Matelaser, Inc. have in the registry?
The registry currently lists 2 devices for Matelaser, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Matelaser, Inc.'s devices?
Among its 2 most recently registered devices, Matelaser, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Matelaser, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Matelaser, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Matelaser, Inc. in the registry?
The most recently registered devices listed for Matelaser, Inc. include MateLaser Medical Laser Therapy Systems (ML-HIL-30, ML-HIL-60) and MateLaser Medical Diode Laser Systems (ML-DLS-30).