Celanese Acetate Co.
Country not established
- Devices
- 1
What Celanese Acetate Co. makes
Celanese Acetate Co. manufactures the JOAN II, a surgical mesh device used in hernia repair procedures.
The JOAN II is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Joan Ii Ref K982648
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Celanese Acetate Co. have in the registry?
The registry currently lists 1 device for Celanese Acetate Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Celanese Acetate Co.'s devices?
Among its 1 most recently registered device, Celanese Acetate Co. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Celanese Acetate Co. in the registry?
The most recently registered devices listed for Celanese Acetate Co. include JOAN II.