Innotherapy, Inc.
South KoreaFDA applicant, unverified
- Devices
- 1
What Innotherapy, Inc. makes
Innotherapy, Inc. manufactures the InnoSEAL Hemostatic Pad, a device designed to control bleeding by applying pressure and promoting clotting at wound sites.
The InnoSEAL Hemostatic Pad is classified as a Class II (U) device under FDA regulations and is listed via a 510(k) clearance. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
InnoSEAL Hemostatic Pad Ref K161013
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Innotherapy, Inc. have in the registry?
The registry currently lists 1 device for Innotherapy, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Innotherapy, Inc.'s devices?
Among its 1 most recently registered device, Innotherapy, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Innotherapy, Inc. in the registry?
The most recently registered devices listed for Innotherapy, Inc. include InnoSEAL Hemostatic Pad.