Adobe Ent.
Country not established
- Devices
- 1
What Adobe Ent. makes
Adobe Ent. manufactures surgical and bandage scissors and forceps.
These devices are classified as Class I and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adobe Ent. have in the registry?
The registry currently lists 1 device for Adobe Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adobe Ent.'s devices?
Among its 1 most recently registered device, Adobe Ent. has devices listed in FDA 510(k) (1 device).
What risk classes do Adobe Ent.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Adobe Ent.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Adobe Ent. in the registry?
The most recently registered devices listed for Adobe Ent. include ADOBE ENTERPRISES SURGICAL/BANDAGE SCISSORS FORCEP.