The Lahr Consulting Group, Inc.
Country not established
- Devices
- 1
What The Lahr Consulting Group, Inc. makes
The Lahr Consulting Group, Inc. manufactures the MANI DIA-BURS, a device designed for dental procedures, specifically for creating and shaping burs in dental applications.
The MANI DIA-BURS is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Mani Dia-Burs Ref K913651
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Lahr Consulting Group, Inc. have in the registry?
The registry currently lists 1 device for The Lahr Consulting Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Lahr Consulting Group, Inc.'s devices?
Among its 1 most recently registered device, The Lahr Consulting Group, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do The Lahr Consulting Group, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Lahr Consulting Group, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from The Lahr Consulting Group, Inc. in the registry?
The most recently registered devices listed for The Lahr Consulting Group, Inc. include MANI DIA-BURS.