American Midwest
Country not established
- Devices
- 5
What American Midwest makes
American Midwest manufactures dental composite restorative systems, including light-cure composites and curing devices. Their portfolio includes the ATT-1 Dental Composite Restorative System, AH-1 Light-Cure Dental Composite Restorative, and the Midwest Light Wand for curing composites. Additional products like the AM-40 System and U-Style Adapter support dental restorative procedures.
The company’s devices are regulated under FDA 510(k) clearance, with products classified as Class I and Class II. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Att-1 Dental Composite Restorative Sys Ref K811979
Regimes: 510(k) Registry: 510(k)Am-40 System Ref K821715
Regimes: 510(k) Registry: 510(k)Ah-1 Light-Cure Dental Composite Restor Ref K821895
Regimes: 510(k) Registry: 510(k)Midwest Light Wand Ref K820693
Regimes: 510(k) Registry: 510(k)U-Style Adapter Ref K800735
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Midwest have in the registry?
The registry currently lists 5 devices for American Midwest. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Midwest's devices?
Among its 5 most recently registered devices, American Midwest has devices listed in FDA 510(k) (5 devices).
What risk classes do American Midwest's devices fall under?
Among its 5 most recently registered devices, the classes recorded for American Midwest's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Midwest in the registry?
The most recently registered devices listed for American Midwest include ATT-1 DENTAL COMPOSITE RESTORATIVE SYS, AM-40 SYSTEM, AH-1 LIGHT-CURE DENTAL COMPOSITE RESTOR and MIDWEST LIGHT WAND.