Accutech Medical Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Accutech Medical Technologies, Inc. makes
Accutech Medical Technologies, Inc. manufactures the Endolite Probe, a diagnostic device used in medical imaging, and a range of Powerflex Laser Delivery Devices designed for precise laser tissue treatment. These products are intended for clinical procedures requiring controlled energy delivery or imaging guidance.
The company’s portfolio is regulated under FDA Class II devices, with relevant products listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Accutech Endolite Probe Ref K061025
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Accutech Medical Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Accutech Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Accutech Medical Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Accutech Medical Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Accutech Medical Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Accutech Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Accutech Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Accutech Medical Technologies, Inc. include ACCUTECH ENDOLITE PROBE and ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES.