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Sign in to claim this brandIngenplast S.A.
Argentina·AR-MF-000037702
Last updated September 17, 2026
About
INGENPLAST is a leading company in Argentina, dedicated for over 40 years to the design and development of Engineering Plastics. Born as a single-person undertaking, our plant is now supported by ISO 9001: 2015 and the National Institute of Industrial Technology (INTI). We have state-of-the-art machines with low-power engine service system and we have our own power group to meet our customers' orders.
Translated from the manufacturer's own website. Source
What Ingenplast S.A. makes
Ingenplast S.A. manufactures prefabricated orthotic insoles, including the Solette Dinamiche Airfeet series in various sizes (N36, N38, N40, N42, N44, N47). These products are designed as non-antimicrobial foot supports for general orthotic use.
The company’s devices fall under EU Class I classification and are registered in the EU’s eudamed database. Ingenplast S.A. is based in Argentina.
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 Ingenplast S.A. manufacture?
Ingenplast S.A. specializes in prefabricated orthotic insoles, specifically the Solette Dinamiche Airfeet series. These devices are designed as non-antimicrobial foot supports intended for general orthotic use, helping to provide foot and lower limb comfort or alignment.
Where is Ingenplast S.A. based, and what is its primary focus?
Ingenplast S.A. is based in Argentina. The company focuses on the design and development of orthotic insoles, leveraging its expertise in engineering plastics to create prefabricated solutions for foot support and alignment.
Are Ingenplast S.A.’s devices listed in any regulatory registries?
Yes, Ingenplast S.A.’s devices are registered in the EU’s eudamed database. This registry is used to track medical devices authorized for placement on the European market, ensuring transparency and traceability.
How are Ingenplast S.A.’s devices classified under EU regulations?
Ingenplast S.A.’s devices fall under EU Class I classification. This classification is typically assigned to low-risk medical devices, such as prefabricated orthotic insoles, which pose minimal risk to patients when used as intended.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Argentina
- Address
- 35, Primera Junta, Turdera, Argentina
- Website
- ingenplast.com
- —
- —
- [email protected]
- Phone
- +39 3663129736
- PRRC Contact
- Santiago Daniel Nunez Romagnoli
- EUDAMED SRN
- AR-MF-000037702
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (7)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Solette Dinamiche Airfeet N36 | Plantilla 36 | EUDAMED | Class I | Active |
| Solette Dinamiche Airfeet | Plantilla 33 | EUDAMED | Class I | Active |
| Solette Dinamiche Airfeet N38 | Plantilla 38 | EUDAMED | Class I | Active |
| Solette Dinamiche Airfeet N47 | Plantilla 47 | EUDAMED | Class I | Active |
| Solette Dinamiche Airfeet N42 | Plantilla 42 | EUDAMED | Class I | Active |
| Solette Dinamiche Airfeet N44 | Plantilla 44 | EUDAMED | Class I | Active |
| Solette Dinamiche Airfeet N40 | Plantilla 40 | EUDAMED | Class I | Active |
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Authorised Representatives
- Epit Srl IT
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