Biomonde
Country not established
- Devices
- 2
What Biomonde makes
Biomonde manufactures larval debridement therapy products, including larval formulations (100, 200, and 300 units) and sterile biobags (sizes 50, 100, 200, 300, and 400). These products are designed for wound care to remove necrotic tissue through controlled larval activity.
The company’s products fall under FDA Class II (U) devices and are listed via 510(k) clearance. They are based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomonde have in the registry?
The registry currently lists 2 devices for Biomonde. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomonde's devices?
Among its 2 most recently registered devices, Biomonde has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Biomonde in the registry?
The most recently registered devices listed for Biomonde include LARVAL DEBRIDEMENT THERAPY PRODUCTS - LARVAE 100/200/300 AND BIOBAG 50/100/200/300/400 and LARVAL DEBRIDEMENT THERAPY PRODUCTS - BIOBAG 50/100/200/300/400.