North America BioPharma
Country not established
- Devices
- 2
What North America BioPharma makes
North America BioPharma produces medicinal leeches for therapeutic use, primarily in procedures requiring blood flow restoration or wound healing.
Their medicinal leeches are classified as Class II (U) devices in the U.S. and are listed under the FDA’s 510(k) pathway. The company operates within the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Medicinal Leeches Ref K132958
Regimes: 510(k) Registry: 510(k)Medicinal Leeches Ref K040187
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does North America BioPharma have in the registry?
The registry currently lists 2 devices for North America BioPharma. Devices recorded under merged duplicate company entries are counted once.
Which registries list North America BioPharma's devices?
Among its 2 most recently registered devices, North America BioPharma has devices listed in FDA 510(k) (2 devices).
What are the newest devices from North America BioPharma in the registry?
The most recently registered devices listed for North America BioPharma include MEDICINAL LEECHES.