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Sign in to claim this brandEOS BIOTEK, INC.
US
Last updated May 24, 2026
What EOS BIOTEK, INC. makes
EOS BIOTEK, INC. manufactures non-sterile bone-screw internal spinal fixation systems designed for surgical spinal stabilization. The company’s portfolio includes the VICEROY Spinal System, which is intended for internal fixation of the spine using screws and other hardware components.
The VICEROY Spinal System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- torreyspineusa.com
- —
- —
- [email protected]
- Phone
- +1-858-345-5840
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 689605712
Catalogue (63)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| VICEROY Spinal System | V-0400 5550 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0201 150 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0200 7550 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0400 7540 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0200 5535 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0200 5550 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0400 5540 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0400 6540 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0202 080 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0202 075 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0400 6535 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0400 6545 | FDA UDI | Class II | Active |
| VICEROY Spinal System | V-0202 085 | FDA UDI | Class II | Active |
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