Amisplint
Country not established
- Devices
- 1
What Amisplint makes
Amisplint manufactures oral sponges, which are designed for oral hygiene and post-surgical care, aiding in wound management and debris removal in the oral cavity.
The company’s oral sponge is classified under FDA’s 510(k) pathway and is listed in the U.S. regulatory registry. The device is intended for use within the oral cavity and adheres to U.S. medical device regulations.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Oral Sponge Ref K823136
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amisplint have in the registry?
The registry currently lists 1 device for Amisplint. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amisplint's devices?
Among its 1 most recently registered device, Amisplint has devices listed in FDA 510(k) (1 device).
What are the newest devices from Amisplint in the registry?
The most recently registered devices listed for Amisplint include ORAL SPONGE.