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US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 1824 COLONIAL VILLAGE LN, Lancaster, PA, 17601
- Website
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
- —
- FDA FEI Number
- 3013921069
- DUNS Number
- 080551837
Catalogue (443)
Page 9 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Keos Lumbar Instrument | Trial Spacer, 10mm, QC, Straight, 23L x 10W | FDA UDI | Class I | Active |
| Anterior Cervical IBFD | 11D x 13W x 06H x 0L, PEEK | FDA UDI | Class II | Active |
| Anterior Cervical IBFD | 11D x 13W x 11H x 7L, PEEK | FDA UDI | Class II | Active |
| Anterior Cervical IBFD | 12D x 14W x 08H x 7L, PEEK | FDA UDI | Class II | Active |
| Keos Lumbar Instrument | Trial Spacer, 14mm, QC, Straight, 23L x 10W | FDA UDI | Class I | Active |
| Keos Lumbar Instrument | Trial Spacer, 14mm, QC, Straight, 23L x 8W | FDA UDI | Class I | Active |
| Keos Lumbar Instrument | Curette, Left, 6mm x 10mm, Serrated, Bayoneted | FDA UDI | Class I | Active |
| Anterior Cervical IBFD | 12D x 14W x 08H x 4L, PEEK | FDA UDI | Class II | Active |
| Keos Lumbar Instrument | Trial Spacer, 10mm, QC, Straight, 28L x 10W | FDA UDI | Class I | Active |
| Keos Anterior Cervical Case/Caddy | Caddy Assy EX, 11D x 13W x 0L, PEEK-HA | FDA UDI | Class I | Active |
| Keos Lumbar Case/Caddy | Implant Case, Lumbar IBFD System, w/ Lid | FDA UDI | Class I | Active |
| Anterior Cervical IBFD | 11D x 13W x 05H x 7L, PEEK | FDA UDI | Class II | Active |
| Keos Lumbar Instrument | Curette, Left, 6mm x 10mm, Bayoneted | FDA UDI | Class I | Active |
| Keos Lumbar Instrument | Lamina Spreader, 279mm, 51mm Jaw Opening | FDA UDI | Class I | Active |
| Keos Anterior Cervical Case/Caddy | Caddy Assy EX, 14D x 16W x 4L, PEEK-HA | FDA UDI | Class I | Active |
| Anterior Cervical IBFD | 14D x 16W x 11H x 7L, PEEK-HA | FDA UDI | Class II | Active |
| Anterior Cervical IBFD | 16D x 18W x 12H x 4L, PEEK | FDA UDI | Class II | Active |
| Anterior Cervical IBFD | 12D x 14W x 06H x 4L, PEEK | FDA UDI | Class II | Active |
| Keos Lumbar Instrument | Box Chisel, 7H | FDA UDI | Class I | Active |
| Keos Lumbar Instrument | Trial Spacer, 7mm, QC, Straight, 23L x 10W | FDA UDI | Class I | Active |
| Anterior Cervical IBFD EX | 14D x 16W x 09H x 7L, PEEK-HA | FDA UDI | Class II | Active |
| Anterior Cervical IBFD EX | 12D x 14W x 06H x 7L, PEEK-HA | FDA UDI | Class II | Active |
| Keos Lumbar Instrument | Curette, Ring, Straight, 6mm, Serrated | FDA UDI | Class I | Active |
| Anterior Cervical IBFD | 14D x 16W x 11H x 7L, PEEK | FDA UDI | Class II | Active |
| Keos Lumbar Instrument | T-Handle, QC, 1/4" Square Adapter | FDA UDI | Class I | Active |
| Anterior Cervical IBFD | 14D x 16W x 05H x 4L, PEEK | FDA UDI | Class II | Active |
| Keos Lumbar Instrument | Pituitary Rongeur, 4x10mm, Straight, w/ Teeth | FDA UDI | Class I | Active |
| Anterior Cervical IBFD EX | 12D x 14W x 12H x 7L, PEEK-HA | FDA UDI | Class II | Active |
| Keos Lumbar Instrument | Curette, Ring, Right, 6mm, Serrated | FDA UDI | Class I | Active |
| Keos Lumbar Instrument | Trial Spacer, 13mm, QC, Straight, 28L x 10W | FDA UDI | Class I | Active |
| Anterior Cervical IBFD EX | 12D x 14W x 09H x 7L, PEEK-HA | FDA UDI | Class II | Active |
| Keos Anterior Cervical Case/Caddy | Caddy Assy, 12D x 14W x 0L, PEEK | FDA UDI | Class I | Active |
| Keos Lumbar Instrument | Trial Spacer, 9mm, QC, Straight, 28L x 10W | FDA UDI | Class I | Active |
| Keos Lumbar Instrument | Curette, Left, 6mm x 10mm | FDA UDI | Class I | Active |
| Anterior Cervical IBFD | 12D x 14W x 12H x 7L, PEEK-HA | FDA UDI | Class II | Active |
| Anterior Cervical IBFD | 16D x 18W x 08H x 7L, PEEK | FDA UDI | Class II | Active |
| Keos Anterior Cervical Case/Caddy | Caddy Assy, 12D x 14W x 4L, PEEK-HA | FDA UDI | Class I | Active |
| Keos Lumbar Instrument | Rotating Distractor, QC, 14mm | FDA UDI | Class I | Active |
| Anterior Cervical IBFD | 11D x 13W x 08H x 4L, PEEK | FDA UDI | Class II | Active |
| Keos Lumbar IBFD | K193174 | FDA 510(k) | Class II | Active |
| Keos Lumbar IBFD | K160631 | FDA 510(k) | Class II | Active |
| Keos Lumbar IBFD | K163386 | FDA 510(k) | Class II | Active |
| Keos Anterior Cervical Interbody Fusion Device System | K212450 | FDA 510(k) | Class II | Active |
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