American Design Group, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What American Design Group, Inc. makes
American Design Group, Inc. manufactures bone plugs, including vented intramedullary bone plugs, and bone biopsy systems.
The company is based in the United States, and its portfolio includes Class I and Class II medical devices that are listed in the FDA 510(k) registry.
Catalogue
Adg Bone Plug Ref K902615
Regimes: 510(k) Registry: 510(k)Adg Intramedullary Bone Plug - Vented Ref K911717
Regimes: 510(k) Registry: 510(k)Adg Bone Biopsy System Ref K890722
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Design Group, Inc. have in the registry?
The registry currently lists 3 devices for American Design Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Design Group, Inc.'s devices?
Among its 3 most recently registered devices, American Design Group, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do American Design Group, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for American Design 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 American Design Group, Inc. in the registry?
The most recently registered devices listed for American Design Group, Inc. include ADG BONE PLUG, ADG INTRAMEDULLARY BONE PLUG - VENTED and ADG BONE BIOPSY SYSTEM.