Actech Advanced Clinical Technologies, Inc.
Country not established
- Devices
- 1
What Actech Advanced Clinical Technologies, Inc. makes
Actech Advanced Clinical Technologies, Inc. manufactures the PERIOCHECK™ Enzyme Activity Test Kit, a diagnostic device used to measure enzyme activity in periodontal disease assessment. This kit aids in evaluating gingival crevicular fluid to support clinical diagnosis and treatment planning for periodontal conditions.
The PERIOCHECK™ Enzyme Activity Test Kit is classified as a Class III medical device in the US and is listed under the FDA’s Premarket Approval (PMA) pathway. The company is headquartered in the United States.
Catalogue
Periocheck Tm Enzyme Activity Test Kit Ref P870059
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Actech Advanced Clinical Technologies, Inc. have in the registry?
The registry currently lists 1 device for Actech Advanced Clinical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Actech Advanced Clinical Technologies, Inc.'s devices?
Among its 1 most recently registered device, Actech Advanced Clinical Technologies, Inc. has devices listed in FDA PMA (1 device).
What risk classes do Actech Advanced Clinical Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Actech Advanced Clinical Technologies, Inc.'s devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Actech Advanced Clinical Technologies, Inc. in the registry?
The most recently registered devices listed for Actech Advanced Clinical Technologies, Inc. include PERIOCHECK TM ENZYME ACTIVITY TEST KIT.