Snore - Ezzer
Country not established
- Devices
- 2
What Snore - Ezzer makes
The company manufactures oral appliances designed to reduce snoring, including custom-fitted mouthpieces like the DR. B'S MOUTHPIECE (Model 32129-10002) and the SNORE-EZZER, which position the jaw to alter airway dynamics during sleep.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The manufacturer operates from the United States.
Catalogue
Dr. B's Mouthpiece, Model 32129-10002 Ref K991948
Regimes: 510(k) Registry: 510(k)Snore-Ezzer Ref K974531
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Snore - Ezzer have in the registry?
The registry currently lists 2 devices for Snore - Ezzer. Devices recorded under merged duplicate company entries are counted once.
Which registries list Snore - Ezzer's devices?
Among its 2 most recently registered devices, Snore - Ezzer has devices listed in FDA 510(k) (2 devices).
What risk classes do Snore - Ezzer's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Snore - Ezzer's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Snore - Ezzer in the registry?
The most recently registered devices listed for Snore - Ezzer include DR. B'S MOUTHPIECE, MODEL 32129-10002 and SNORE-EZZER.