Acculaser, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Acculaser, Inc. makes
Acculaser, Inc. manufactures low-level laser therapy devices, including the ACCULASER PRO4 and ACCULASER PRO, designed for therapeutic applications in soft tissue treatment and pain management.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Acculaser PRO4 Ref K023060
Regimes: 510(k) Registry: 510(k)Acculaser Pro Low Level Laser Therapy Device Ref K020657
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acculaser, Inc. have in the registry?
The registry currently lists 2 devices for Acculaser, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acculaser, Inc.'s devices?
Among its 2 most recently registered devices, Acculaser, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Acculaser, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Acculaser, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acculaser, Inc. in the registry?
The most recently registered devices listed for Acculaser, Inc. include ACCULASER PRO4 and ACCULASER PRO LOW LEVEL LASER THERAPY DEVICE.