Acorn Group, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Acorn Group, Inc. makes
Acorn Group, Inc. manufactures medical devices including irrigation and suction apparatus for surgical procedures, the Visiraser for ophthalmic applications, cervical spine fixation hardware such as titanium bone screws and top cervical spine plates, and laryngoscopes for airway visualization.
Their portfolio includes Class I and Class II devices, with products listed under the FDA’s 510(k) clearance process. The company operates from the United States.
Catalogue
Irrigation And Suction Apparatus Ref K900430
Regimes: 510(k) Registry: 510(k)Visiraser Ref K904126
Regimes: 510(k) Registry: 510(k)Top Cervical Spine Plates & Titanium Bone Screws Ref K914362
Regimes: 510(k) Registry: 510(k)Laryngoscope Ref K912905
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acorn Group, Inc. have in the registry?
The registry currently lists 4 devices for Acorn Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acorn Group, Inc.'s devices?
Among its 4 most recently registered devices, Acorn Group, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Acorn Group, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Acorn Group, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Acorn Group, Inc. in the registry?
The most recently registered devices listed for Acorn Group, Inc. include IRRIGATION AND SUCTION APPARATUS, VISIRASER, TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWS and LARYNGOSCOPE.