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 E6149S
Salient Ref PEI151470
Osseous Ref EA91053
Osseous Ref EI0982WA
Osseous Ref E91006
Osseous Ref EI0953
Osseous Ref EA91034
Osseous Ref EI07
Osseous Ref EA91003
Osseous Ref EI0951
Osseous Ref EA91001
Osseous Ref EI02
Osseous Ref EA910017
Osseous Ref EI0953
Osseous Ref EA91057
Salient Ref PEI1220100
Osseous Ref E3148FS
Orleon Ref FI1230100
Orleon Ref F3148FTP
Orleon Ref F3147L
Osseous Ref EI150460
Salient Ref PEI1235140
Osseous Ref EI140870
Osseous Ref EI1350120R
Osseous Ref EI1340140R
Salient Ref PE7164
Osseous Ref EI1630250
Osseous Ref EI1220140
Osseous Ref EI2150FD
Osseous Ref E3131618
Osseous Ref EI1514100
Osseous Ref EI2170SS
Osseous Ref E2138T
Osseous Ref EI2140FD
Salient Ref PE6149L
Osseous Ref EI150480
Orleon Ref FI140770
Osseous Ref EI151060
Osseous Ref EI1520100
Osseous Ref EI143080
Salient Ref PE2114B
Osseous Ref E3111255F
Osseous Ref E3131418
Osseous Ref EI1340160R
Orleon Ref F7165
Osseous Ref EI1330160R
Osseous Ref E3110836S
Osseous Ref EI1240140
Osseous Ref EI1230120
Osseous Ref E3145L
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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