Aci, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Aci, Inc. makes
Aci, Inc. manufactures the GFX Nerve Ablation System and Flexo Dental Resin Material, both of which are Class II medical devices.
The company is based in the US and its devices are listed in the FDA 510(k) registry, indicating they have been cleared for marketing through the premarket notification process.
Catalogue
Gfx Nerve Ablation System Ref K063753
Regimes: 510(k) Registry: 510(k)Flexo Dental Resin Material Ref K061501
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aci, Inc. have in the registry?
The registry currently lists 2 devices for Aci, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aci, Inc.'s devices?
Among its 2 most recently registered devices, Aci, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Aci, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Aci, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aci, Inc. in the registry?
The most recently registered devices listed for Aci, Inc. include GFX NERVE ABLATION SYSTEM and FLEXO DENTAL RESIN MATERIAL.