Osteogenics Biomedical, Inc. (Formerly Obi Biologi
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- Devices
- 1
What Osteogenics Biomedical, Inc. (Formerly Obi Biologi makes
Osteogenics Biomedical, Inc. manufactures the VITALA porcine-derived collagen membrane, a resorbable barrier used in bone regeneration procedures to support tissue integration and wound healing.
The company’s product portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Vitala Porcine Derived Collagen Membrane Ref K141177
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteogenics Biomedical, Inc. (Formerly Obi Biologi have in the registry?
The registry currently lists 1 device for Osteogenics Biomedical, Inc. (Formerly Obi Biologi. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteogenics Biomedical, Inc. (Formerly Obi Biologi's devices?
Among its 1 most recently registered device, Osteogenics Biomedical, Inc. (Formerly Obi Biologi has devices listed in FDA 510(k) (1 device).
What risk classes do Osteogenics Biomedical, Inc. (Formerly Obi Biologi's devices fall under?
Among its 1 most recently registered device, the classes recorded for Osteogenics Biomedical, Inc. (Formerly Obi Biologi's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osteogenics Biomedical, Inc. (Formerly Obi Biologi in the registry?
The most recently registered devices listed for Osteogenics Biomedical, Inc. (Formerly Obi Biologi include VITALA PORCINE DERIVED COLLAGEN MEMBRANE.