A.L. Miller, Inc.
Country not established
- Devices
- 1
What A.L. Miller, Inc. makes
A.L. Miller, Inc. manufactures the EXPAND. RETENTION endosseous implant, a device designed for internal fixation and retention within bone structures, likely used in orthopedic or maxillofacial applications.
The company’s portfolio is regulated under FDA Class II devices, with the EXPAND. RETENTION endosseous implant listed via a 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Expand. Retention Endosseous Implant Ref K771858
510(k) 510(k)
Frequently asked questions
How many devices does A.L. Miller, Inc. have in the registry?
The registry currently lists 1 device for A.L. Miller, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list A.L. Miller, Inc.'s devices?
Among its 1 most recently registered device, A.L. Miller, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do A.L. Miller, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for A.L. Miller, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A.L. Miller, Inc. in the registry?
The most recently registered devices listed for A.L. Miller, Inc. include EXPAND. RETENTION ENDOSSEOUS IMPLANT.