EON MEDITECH PVT. LTD
India IN-MF-000014457 Last updated 21 Oct 2026
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- Devices
- 582
- Registries
- EUDAMEDGUDID
- FDA recalls
- 0
Catalogue
Osseous Ref EI2135FD
Orleon Ref FI2201
Orleon Ref FI151480
Osseous Ref EI1330120R
Osseous Ref EI140470
Orleon Ref FI150670
Osseous Ref E7189
Osseous Ref E7183
Osseous Ref EI141270
Osseous Ref EI1350120L
Salient Ref PE1105
Orleon Ref F7161
Salient Ref PEI1220160
Osseous Ref E2116
Osseous Ref E7185
Osseous Ref EI1230100
Salient Ref PE6149L
Orleon Ref F31030
Salient Ref PE3148FT
Osseous Ref EI1350160L
Osseous Ref E3148ST
Osseous Ref E3110936F
Osseous Ref EI2110FD
Osseous Ref E7168
Osseous Ref E7191
Osseous Ref EI141770
Osseous Ref E2123
Osseous Ref EI1830150
Salient Ref PE2114BW
Orleon Ref FI1520100
Orleon Ref F3115L
Osseous Ref E7192
Orleon Ref F7164
Orleon Ref FI0968
Osseous Ref E2112
Osseous Ref EI150470
Osseous Ref E3111236F
Salient Ref PEI1250140
Osseous Ref EI1325140L
Osseous Ref EI2201
Orleon Ref FI1240140
Osseous Ref EI151460
Salient Ref PE7180
Osseous Ref E3111055F
Osseous Ref E2142
Osseous Ref EI2120FD
Orleon Ref F3148FT
Osseous Ref EI2145CD
Orleon Ref F5150L
Osseous Ref EI2150TC
Showing 151-200 of 582
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What EON MEDITECH PVT. LTD makes
EON Meditech manufactures orthopaedic implants and fixation devices designed for osseous applications, including screws, plates, and related hardware for bone stabilization and reconstruction. Their product line also includes specialized orthopaedic tools and systems for surgical procedures, such as the Salient, Orleon, and other osseous-specific devices.
The company’s portfolio is regulated under EU Medical Device Regulations, with devices classified as Class I, Class IIa, and Class IIb, and is listed in the EUDAMED database. The manufacturer is based in India and adheres to relevant regulatory frameworks for orthopaedic implants and surgical instruments.
Frequently asked questions
What types of medical devices does EON Meditech manufacture?
EON Meditech specializes in orthopaedic implants and fixation devices primarily for osseous (bone-related) applications. Their product line includes screws, plates, and other hardware used in bone stabilization and reconstruction surgeries. Additionally, they produce specialized orthopaedic tools and systems, such as the Salient and Orleon lines, which are designed for surgical procedures involving bone.
Where is EON Meditech based, and what regulatory frameworks do they follow?
EON Meditech is headquartered in India. Their devices are regulated under the EU Medical Device Regulations (MDR) when marketed in the European Union, with classifications spanning Class I, Class IIa, and Class IIb. This classification depends on the risk associated with each specific device, as determined by regulatory authorities.
Are EON Meditech’s devices listed in any regulatory databases?
Yes, EON Meditech’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This database provides transparency on manufacturers, devices, and regulatory information for stakeholders, including healthcare professionals and regulatory bodies.
How are EON Meditech’s devices classified under EU regulations?
EON Meditech’s devices are classified under the EU Medical Device Regulations (MDR) based on their intended purpose and associated risks. For example, osseous implants like screws and plates may fall into Class IIa or Class IIb due to their role in surgical procedures and potential impact on patient safety. Classification ensures appropriate regulatory oversight, with higher-risk devices requiring stricter scrutiny.
What distinguishes EON Meditech’s orthopaedic devices from others in the market?
EON Meditech’s devices are specifically designed for osseous applications, focusing on bone stabilization, reconstruction, and surgical tools tailored for orthopaedic procedures. Their portfolio includes both standard fixation hardware and specialized systems like the Salient and Orleon lines, which are engineered to meet precise clinical needs in orthopaedic surgery. The classification under EU MDR reflects their role in high-risk medical contexts.
Information
- Country
- India
- Address
- Factory: BL 54, 127, 129, Khanpur Road, Mirapur, Kamrej, Surat -394320, Gujarat, India, Surat, India
- Website
- www.eonmeditech.com
- [email protected]
- PRRC contact
- Nirav Khunt
- EUDAMED SRN
- IN-MF-000014457