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Sign in to claim this brandVERTERA, INC.
US
Last updated May 24, 2026
What VERTERA, INC. makes
Vertera, Inc. manufactures polymeric spinal fusion cages designed for sterile surgical use, intended to support spinal stabilization and fusion procedures.
These devices are classified as Class II under FDA regulations and are authorised via 510(k) premarket notifications and the Unique Device Identifier (UDI) system. 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.
Frequently asked questions
What types of medical devices does Vertera, Inc. manufacture?
Vertera, Inc. specializes in polymeric spinal fusion cages intended for sterile surgical use. These devices are primarily designed to aid in spinal stabilization and fusion procedures, helping to support the spine during recovery and healing.
Where is Vertera, Inc. based, and what does that mean for its regulatory oversight?
Vertera, Inc. is based in the United States, which means its devices are subject to FDA regulations. Since the company’s products fall under Class II classification, they undergo premarket review through 510(k) notifications or are tracked via the Unique Device Identifier (UDI) system to ensure compliance with U.S. medical device standards.
Which regulatory registries or databases list Vertera, Inc.’s devices?
Vertera, Inc.’s devices are listed in the FDA’s 510(k) premarket notification database and the Unique Device Identifier (UDI) system. These registries track authorised devices to ensure transparency and compliance with U.S. medical device regulations.
How are Vertera, Inc.’s devices classified under FDA regulations?
Vertera, Inc.’s polymeric spinal fusion cages are classified as Class II devices by the FDA. This classification indicates moderate regulatory oversight, requiring premarket submissions (like 510(k) notifications) or UDI registration to demonstrate safety and effectiveness before commercial distribution.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 078812764
Catalogue (47)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cohere | 1000-00-0616 | FDA UDI | Class II | Active |
| Coalesce | 2000-01-2808 | FDA UDI | Class II | Unknown |
| Cohere | 1000-00-1014 | FDA UDI | Class II | Active |
| Coalesce | 2000-01-2811 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-00-090800 | FDA UDI | Class II | Active |
| Coalesce | 2000-00-101008 | FDA UDI | Class II | Active |
| Coalesce | 22000-00-091008 | FDA UDI | Class II | Active |
| Coalesce | 2000-00-091200 | FDA UDI | Class II | Active |
| Coalesce | 2000-01-2814 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-00-100908 | FDA UDI | Class II | Active |
| Cohere | 1100-01-0001 | FDA UDI | Class I | Unknown |
| Coalesce | 2000-01-3210 | FDA UDI | Class II | Unknown |
| Cohere | 1000-00-0814 | FDA UDI | Class II | Active |
| Cohere | 1000-00-0816 | FDA UDI | Class II | Active |
| Coalesce | 2000-01-2809 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-01-2812 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-00-091108 | FDA UDI | Class II | Active |
| Coalesce | 2000-01-3212 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-00-101208 | FDA UDI | Class II | Unknown |
| Cohere | 1000-00-1016 | FDA UDI | Class II | Active |
| Cohere | 1100-00-0001 | FDA UDI | Class I | Unknown |
| Cohere | 1000-00-0614 | FDA UDI | Class II | Active |
| Coalesce | 2000-01-3214 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-00-100808 | FDA UDI | Class II | Active |
| Cohere | 1100-00-0014 | FDA UDI | Class I | Unknown |
| Coalesce | 2000-01-3209 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-00-091408 | FDA UDI | Class II | Active |
| Coalesce | 2000-01-3216 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-00-091208 | FDA UDI | Class II | Active |
| Coalesce | 2000-00-101408 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-00-090908 | FDA UDI | Class II | Active |
| Coalesce | 2000-00-091100 | FDA UDI | Class II | Active |
| Coalesce | 2000-01-3211 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-00-090808 | FDA UDI | Class II | Active |
| Coalesce | 2000-00-090900 | FDA UDI | Class II | Active |
| Cohere | 1000-00-0716 | FDA UDI | Class II | Active |
| Cohere | 1000-00-0714 | FDA UDI | Class II | Active |
| Coalesce | 2000-00-101108 | FDA UDI | Class II | Active |
| Coalesce | 2000-00-091000 | FDA UDI | Class II | Active |
| Cohere | 1000-00-0916 | FDA UDI | Class II | Active |
| Coalesce | 2000-01-2810 | FDA UDI | Class II | Unknown |
| Coalesce | 2000-01-3208 | FDA UDI | Class II | Active |
| Coalesce | 2000-00-091400 | FDA UDI | Class II | Active |
| Cohere | 1000-00-0914 | FDA UDI | Class II | Active |
| Cohere | 1100-00-0016 | FDA UDI | Class I | Unknown |
| Hedgehog Cervical Interbody Fusion Device | K143685 | FDA 510(k) | Class II | Active |
| Coalesce™ (-Straight, -Convex, -Crescent, -Lateral, -Anterior, or -Oblique) Lumbar Interbody Fusion System | K163506 | FDA 510(k) | Class II | Active |
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