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Sign in to claim this brandKator, LLC
US
Last updated May 30, 2026
What Kator, LLC makes
Kator, LLC manufactures ligament bone anchors, including suture anchors designed for orthopedic fixation. These devices are intended for securing soft tissue to bone, commonly used in shoulder, knee, and ankle surgeries to repair ligaments or tendons.
The company’s products fall under FDA Class II regulation and are listed via 510(k) and UDI pathways. The manufacturer 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 Kator, LLC manufacture?
Kator, LLC specializes in ligament bone anchors, with a focus on suture anchors. These devices are primarily used in orthopedic surgery to attach soft tissues—such as ligaments or tendons—to bone. They are commonly applied in procedures involving the shoulder, knee, or ankle to aid in ligament or tendon repair.
Where is Kator, LLC based?
Kator, LLC is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and compliance with U.S. medical device standards.
How are Kator, LLC’s devices classified by regulatory authorities?
Kator, LLC’s devices are classified as FDA Class II. This classification indicates they pose a moderate risk and require specific regulatory controls, including premarket notifications (510(k)) and unique device identifiers (UDI) to ensure safety and effectiveness.
Which regulatory registries or databases list Kator, LLC’s devices?
Kator, LLC’s devices are listed in the FDA’s 510(k) premarket notification database and the FDA’s Unique Device Identifier (UDI) system. These registries help track and verify the authorization status of medical devices in the U.S. market.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- 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
- 080346102
Catalogue (7)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Kator, Llc | 1030590 | FDA UDI | Class II | Active |
| Kator, Llc | 1030593 | FDA UDI | Class II | Active |
| Kator, Llc | 1030591 | FDA UDI | Class II | Active |
| Kator, Llc | 1030592 | FDA UDI | Class II | Active |
| KATOR Suture Anchor | K173269 | FDA 510(k) | Class II | Active |
| KATOR Suture Anchor | K162386 | FDA 510(k) | Class II | Active |
| KATOR Suture Anchor | K152236 | FDA 510(k) | Class II | Active |
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