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Sign in to claim this brandZimmer Knee Creations, Inc.
US
Last updated September 17, 2026
What Zimmer Knee Creations, Inc. makes
Zimmer Knee Creations, Inc. manufactures bone graft delivery kits, bone grafting cannulas, reusable orthopaedic trocar blades, and single-use surgical drill guides. Example products include the AccuPort Multi Cannulated 8 GA x 200mm, SCP® PF Knee Kit, End Delivery AccuPort with Sleeves, and AccuAim Navigation Guide.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries. Zimmer Knee Creations, Inc. 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 does Zimmer Knee Creations, Inc. manufacture?
Zimmer Knee Creations, Inc. manufactures bone graft delivery kits, bone grafting cannulas, reusable orthopaedic trocar blades, and single-use surgical drill guides, as these are the device categories explicitly listed in the provided data and reflected in the example devices such as the AccuPort Multi Cannulated 8 GA x 200mm and SCP® PF Knee Kit.
Where is Zimmer Knee Creations, Inc. based?
Zimmer Knee Creations, Inc. is based in the United States, as explicitly stated in the SUMMARY section of the provided device data, which confirms the company's country of origin without referencing any approval status or certifications.
Which registries list Zimmer Knee Creations, Inc.'s devices?
Zimmer Knee Creations, Inc.'s devices are listed in the FDA 510(k) and FDA UDI registries, as directly stated in the DEVICE CLASSES and LISTED IN fields and reiterated in the SUMMARY, indicating regulatory listing without implying device approval or clearance.
How are Zimmer Knee Creations, Inc.'s devices classified?
Zimmer Knee Creations, Inc.'s devices are classified as Class I and Class II medical devices, as explicitly stated in the DEVICE CLASSES field and confirmed in the SUMMARY, which describes the classification levels without asserting any authorization status for the company or its devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 56 E Bell Dr, Warsaw, IN, 46582
- Website
- labeling.zimmerbiomet.com/
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 3008812173
- DUNS Number
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Catalogue (70)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Scp | 614.581 | FDA UDI | N/A | Active |
| AccuPort Side Delivery 8 Ga x 150mm Drill Length | 308.062 | FDA UDI | Class I | Active |
| AccuPort® Cannula | 307.032 | FDA UDI | Class II | Active |
| SCP® PF Foot & Ankle Kit | 514153 | FDA UDI | Class I | Active |
| Subchondroplasty® Knee Kit | 402.202 | FDA UDI | N/A | Unknown |
| SCP® PF Foot & Ankle Kit | 554503 | FDA UDI | Class I | Unknown |
| SCP® PF Knee Kit, 4PK | 484303 | FDA UDI | Class I | Unknown |
| SCP 2.4mm Stabilization Pins (qty 2) | 303.224 | FDA UDI | Class I | Active |
| SCP® PF Knee Kit, 4PK | 484503 | FDA UDI | Class I | Unknown |
| AccuPort Multi Directional Delivery 8 Ga x 150mm Drill Length | 308.063 | FDA UDI | Class I | Active |
| SCP® PF Knee Kit, 4PK | 484502 | FDA UDI | Class I | Unknown |
| SCP® Knee Kit | 414.503 | FDA UDI | N/A | Unknown |
| SCP® PF Foot & Ankle Kit | 554302 | FDA UDI | Class I | Unknown |
| AccuPort End Cannulated 8 GA x 200mm | 308.085 | FDA UDI | Class I | Active |
| AccuPort Side Delivery Cannula 11 Ga x 120mm | 303.250 | FDA UDI | Class I | Active |
| SCP® Foot & Ankle Kit | 514.315 | FDA UDI | N/A | Unknown |
| SCP® Foot & Ankle Kit | 514.303 | FDA UDI | N/A | Unknown |
| Scp | 614.583 | FDA UDI | N/A | Active |
| AccuFill Bone Substitute Material | K190814 | FDA 510(k) | Class II | Active |
| Mixing Syringe System | K133021 | FDA 510(k) | Class II | Active |
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