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Sign in to claim this brandImplanet
US
Last updated May 23, 2026
What Implanet makes
Implanet manufactures spinal fixation devices, including trans-facet screws, internal fixation rods, polymeric interbody fusion cages, and cable tensioners for spinal stabilization. Their portfolio also includes cruciate-retaining total knee prostheses, orthopaedic surgical kits, and reusable instrument trays for orthopaedic procedures.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Implanet 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 Implanet manufacture?
Implanet specializes in spinal and orthopaedic devices. Their portfolio includes systems for spinal stabilization like trans-facet screws, internal spinal fixation rods, polymeric interbody fusion cages, and cable tensioners. They also produce cruciate-retaining total knee prostheses, reusable orthopaedic surgical kits, and instrument trays designed for orthopaedic procedures. These devices are primarily used in spinal and joint surgeries to provide structural support and promote healing.
Where is Implanet based?
Implanet is headquartered in the United States. The company’s location is relevant for regulatory compliance, as it operates under the jurisdiction of the U.S. Food and Drug Administration (FDA). This means their devices must adhere to FDA guidelines and regulations for classification, listing, and post-market surveillance.
Which regulatory registries list Implanet’s devices?
Implanet’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a standardized approach to identify medical devices throughout their distribution and helps ensure traceability, regulatory compliance, and transparency in the healthcare system. Listing in this database is required for Class I and Class II devices in the U.S.
How are Implanet’s devices classified by the FDA?
Implanet’s devices are classified under the FDA’s Class I and Class II categories. Class I devices generally pose the lowest risk and are typically exempt from premarket notification (510(k)) requirements, while Class II devices require special controls to ensure their safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body area it interacts with, such as spinal or joint stabilization.
Why does the classification of Implanet’s devices matter?
The FDA classification determines the regulatory pathway a device must follow before it can be marketed. For example, Class II devices like some of Implanet’s spinal fixation systems require premarket submissions to demonstrate compliance with FDA regulations, ensuring they meet performance standards and safety requirements. This classification helps healthcare providers and regulators assess the risk associated with the device, influencing how it is used in clinical settings and monitored post-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
- 291993439
Catalogue (1134)
Page 12 of 23| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| JAZZ System | Jazz Screw - Polyaxial Screw Dia.5.5 L40 | FDA UDI | Class II | Active |
| Madison | Madison BL Stylus Stand 1 | FDA UDI | Class I | Active |
| JAZZ System | JAZZ PF Band Reducer | FDA UDI | Class II | Active |
| Implanet Spine System | Ø5.0 Tap | FDA UDI | Class I | Active |
| JAZZ System | Jazz Screw - Monoaxial Screw Dia.6 L55 | FDA UDI | Class II | Active |
| Implanet Spine System | Straight Union Rod | FDA UDI | Class II | Active |
| JAZZ System | JAZZ Claw – Pre-bent Rod Dia. 4/5.5 L70 - CoCr | FDA UDI | Class II | Active |
| Madison | Tibial punch - S3-4-5 - Cemented | FDA UDI | Class II | Active |
| Implanet Spine System | Pre-bent Union Rod | FDA UDI | Class II | Active |
| Implanet Spine System | Dual Monoaxial Screw | FDA UDI | Class II | Active |
| JAZZ System | Connector Kit | FDA UDI | Class II | Active |
| Implanet Spine System | Sacral Awl | FDA UDI | Class I | Active |
| Implanet Spine System | Polyaxial Pedicle Screw | FDA UDI | Class II | Active |
| JAZZ System | JAZZ Passer Band | FDA UDI | Class II | Active |
| JAZZ System | Jazz Screw - Monoaxial Screw Dia.8 L60 | FDA UDI | Class II | Active |
| Madison | Headed pin - Dia. 3.2mm / L2 | FDA UDI | Class I | Active |
| Implanet Spine System | Sub S1 Connector Screw | FDA UDI | Class II | Active |
| JAZZ System | Straight Passer – 15mm | FDA UDI | Class II | Active |
| Implanet Spine System | Prebent Union Rod | FDA UDI | Class II | Active |
| Implanet Spine System | Straight Union Rod | FDA UDI | Class II | Active |
| JAZZ System | JAZZClaw – Hook Right Large | FDA UDI | Class II | Active |
| Madison | UC insert trial size 7 - 18mm | FDA UDI | Class II | Active |
| JAZZ System | Tensioner Gen. II - Universal 135° Stem | FDA UDI | Class II | Active |
| Implanet Spine System | Straight Union Rod | FDA UDI | Class II | Active |
| Implanet Spine System | Prebent Union Rod | FDA UDI | Class II | Active |
| Squale | 580009 | FDA UDI | Class I | Active |
| Jazz Frame | JAZZ Frame – Straight Rod Dia. 6.0 L600 | FDA UDI | Class II | Active |
| Madison | Universal UC insert Size 8 - 10 mm | FDA UDI | Class II | Active |
| Implanet Spine System | Monoaxial Pedicle Screw | FDA UDI | Class II | Active |
| Implanet Spine System | Hook pusher | FDA UDI | Class I | Active |
| Madison | Smooth broach - Dia 3.2mm / L2 | FDA UDI | Class I | Active |
| JAZZ System | Straight Passer – 25mm | FDA UDI | Class II | Active |
| Implanet Spine System | Dual Polyaxial Screw | FDA UDI | Class II | Active |
| Jazz Spinal System | 634828 | FDA UDI | Class II | Active |
| Squale | 380008 | FDA UDI | Class II | Active |
| JAZZ System | Jazz Screw - Polyaxial Screw Dia.5 L60 | FDA UDI | Class II | Active |
| Implanet Spine System | Straight Union Rod CoCr | FDA UDI | Class II | Active |
| Implanet Spine System | Straight Union Rod CoCr | FDA UDI | Class II | Active |
| Madison | Madison Pins quick connector | FDA UDI | Class I | Active |
| Madison | Tibial preparation drill | FDA UDI | Class II | Active |
| JAZZ System | Jazz Screw - Monoaxial Screw Dia.8 L45 | FDA UDI | Class II | Active |
| Implanet Spine System | Straight Union Rod | FDA UDI | Class II | Active |
| Madison | Cemented CR femoral component S5 L | FDA UDI | Class II | Active |
| JAZZ System | JAZZ PF 6mm/JAZZ band Set | FDA UDI | Class II | Active |
| Jazz Frame | JAZZ Frame - T-Bar Dia.4,5 L25 | FDA UDI | Class II | Active |
| JAZZ System | Jazz Screw - Monoaxial Screw Dia.5 L45 | FDA UDI | Class II | Active |
| JAZZ System | JAZZ Apex Derotator | FDA UDI | Class I | Active |
| Implanet Spine System | Straight Union Rod | FDA UDI | Class II | Active |
| Madison | LB Femoral cutting guide – S2 | FDA UDI | Class I | Active |
| Implanet Spine System | Prebent Union Rod | FDA UDI | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Implanet Martillac Nouvelle-Aquitaine · FR FEI 3007675554