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US
Last updated May 30, 2026
What KASIOS makes
KASIOS manufactures synthetic bone graft products, including OSTEOPORE TCP and DUOWEDGE, which are used in orthopedic applications.
The company's devices are classified as Class II and are listed in the FDA 510(k) and FDA UDI registries. KASIOS is based in the US.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What products does KASIOS manufacture?
KASIOS manufactures synthetic bone graft products, including OSTEOPORE TCP and DUOWEDGE, which are used in orthopedic applications. These devices are designed to support bone regeneration and repair in surgical procedures.
Where is KASIOS based?
KASIOS is based in the United States. The company operates within the US, developing and manufacturing its synthetic bone graft products for medical use in orthopedic applications.
Which regulatory registries list KASIOS devices?
KASIOS devices are listed in the FDA 510(k) and FDA UDI registries. These listings indicate that the company's products meet certain regulatory requirements for medical devices in the US market.
How are KASIOS devices classified?
KASIOS devices are classified as Class II medical devices. This classification indicates they require special controls for safety and effectiveness, but are generally considered lower risk than Class III devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- kasios.com
- —
- —
- [email protected]
- Phone
- +0033534273323
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 572720055
Catalogue (51)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Duowedge Synthetic Bone Substitute | K073214 | FDA 510(k) | Class II | Active |
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