Martin D. Lerman
Country not established
- Devices
- 1
What Martin D. Lerman makes
Martin D. Lerman manufactures the Aqualizer mouthpiece, which is an oral appliance designed for dental use.
The company is based in the United States, and its product is classified as a Class I medical device listed in the FDA 510(k) database.
Catalogue
Aqualizer Mouthpiece Ref K831793
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Martin D. Lerman have in the registry?
The registry currently lists 1 device for Martin D. Lerman. Devices recorded under merged duplicate company entries are counted once.
Which registries list Martin D. Lerman's devices?
Among its 1 most recently registered device, Martin D. Lerman has devices listed in FDA 510(k) (1 device).
What risk classes do Martin D. Lerman's devices fall under?
Among its 1 most recently registered device, the classes recorded for Martin D. Lerman's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Martin D. Lerman in the registry?
The most recently registered devices listed for Martin D. Lerman include AQUALIZER MOUTHPIECE.