Jeffrey H. Attlin
Country not established
- Devices
- 1
What Jeffrey H. Attlin makes
The company designs and manufactures a remoldable craniomandibular appliance, a customizable oral device used for managing temporomandibular joint disorders (TMD) or related dental conditions.
This product is classified as a Class I medical device under FDA regulations and is listed in the 510(k) clearance registry. The manufacturer operates from the United States.
Catalogue
Remoldable Craniomandibular Appliance Ref K833455
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jeffrey H. Attlin have in the registry?
The registry currently lists 1 device for Jeffrey H. Attlin. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jeffrey H. Attlin's devices?
Among its 1 most recently registered device, Jeffrey H. Attlin has devices listed in FDA 510(k) (1 device).
What risk classes do Jeffrey H. Attlin's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jeffrey H. Attlin's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jeffrey H. Attlin in the registry?
The most recently registered devices listed for Jeffrey H. Attlin include REMOLDABLE CRANIOMANDIBULAR APPLIANCE.