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US
Last updated May 24, 2026
What DILON TECHNOLOGIES FRANCE makes
Dilon Technologies France manufactures collagen-based haemostatic agents designed to control bleeding during surgical procedures. Their products include laparoscopic applicators and bellows systems, specifically for use in minimally invasive surgeries where precise haemostasis is required.
These devices are classified as Class III under regulatory frameworks, requiring stringent pre-market approval processes. They are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with US medical device regulations. The company 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 Dilon Technologies France manufacture?
Dilon Technologies France specializes in collagen-based haemostatic agents, specifically non-antimicrobial types. These devices are designed to stop bleeding during surgical procedures, particularly in minimally invasive surgeries like laparoscopy. Their most common products include applicators and bellows systems, such as the HEMOBLAST Bellows Laparoscopic Applicator and HEMOBLAST Bellows, which help achieve precise haemostasis in controlled surgical environments.
Where is Dilon Technologies France based, and what is its primary focus?
Dilon Technologies France is based in the United States. The company focuses on developing collagen haemostatic agents tailored for surgical settings where bleeding control is critical. Their solutions are engineered to support minimally invasive procedures, ensuring effective haemostasis with specialised applicators and systems.
Which regulatory registries list Dilon Technologies France’s devices?
Dilon Technologies France’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance with US medical device regulations, allowing for clear identification and tracking of their Class III haemostatic agents, such as the HEMOBLAST products.
How are Dilon Technologies France’s devices classified under regulatory standards?
Dilon Technologies France’s haemostatic agents fall under Class III classification. This classification is reserved for devices that support or sustain human life, are of substantial importance in preventing impairment of human health, or present a potential unreasonable risk of illness or injury. As a result, these devices undergo rigorous pre-market approval processes to ensure safety and efficacy.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- xx.xx
- —
- —
- [email protected]
- Phone
- +33486573610
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 279346203
Catalogue (24)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Covamax | MCG 13 34 AA | FDA UDI | Class II | Unknown |
| Cova Ortho Nerve | MCG 13 34 AD | FDA UDI | Class II | Unknown |
| Covaortho-Nerve | MCG 12 23 V | FDA UDI | Class II | Unknown |
| Covaortho-Nerve | MCG 13 34 V | FDA UDI | Class II | Unknown |
| HEMOBLAST Bellows Laparoscopic Applicator | LAP01-US | FDA UDI | Class III | Active |
| Covaortho-Nerve | MCG 15 68 V | FDA UDI | Class II | Unknown |
| Covamesh | MSH 09 1510 V | FDA UDI | Class II | Unknown |
| Covamesh | MSH 10 2015 V | FDA UDI | Class II | Unknown |
| HEMOBLAST Bellows | BQF02 | FDA UDI | Class III | Active |
| Covaortho-Nerve | MCG 14 46 V | FDA UDI | Class II | Unknown |
| Cova Ortho Nerve | MCG 11 12 AD | FDA UDI | Class II | Unknown |
| Salvin Renovix | MCG 13 34 U | FDA UDI | Class II | Unknown |
| Salvin Renovix | MCG 12 23 U | FDA UDI | Class II | Unknown |
| Cova Ortho Nerve | MCG 14 46 AD | FDA UDI | Class II | Unknown |
| Cova Ortho Nerve | MCG 12 23 AD | FDA UDI | Class II | Unknown |
| Salvin Renovix | MCG 11 12 U | FDA UDI | Class II | Unknown |
| Covamesh | MSH 12 3020 V | FDA UDI | Class II | Unknown |
| Covaortho-Nerve | MCG 11 12 V | FDA UDI | Class II | Unknown |
| Cova Ortho Nerve | MCG 15 68 AD | FDA UDI | Class II | Unknown |
| Covamax | MCG 12 23 AA | FDA UDI | Class II | Unknown |
| Covamesh | MSH 08 D12 V | FDA UDI | Class II | Unknown |
| Covamesh | MSH 11 2520 V | FDA UDI | Class II | Unknown |
| Covamax | MCG 11 12 AA | FDA UDI | Class II | Unknown |
| Covamesh | MSH 13 D16 V | FDA UDI | Class II | Unknown |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Dilon Technologies France SAS St Priest Rhone · FR FEI 3007702492