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Sign in to claim this brandDanmic Global, LLC
United States·US-MF-000021060
Last updated September 17, 2026
What Danmic Global, LLC makes
Danmic Global, LLC manufactures the Aesthesio, a medical device designed for localized anesthetic administration, likely intended for procedural sedation or minor surgical interventions.
The Aesthesio is classified as a Class I medical device and is listed in the EU’s eudamed registry, indicating compliance with EU 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 Danmic Global, LLC manufacture?
Danmic Global, LLC specializes in the Aesthesio, a medical device intended for localized anesthetic administration. This device is likely used in procedural sedation or minor surgical interventions, helping to numb specific areas during medical procedures.
Where is Danmic Global, LLC based?
Danmic Global, LLC is headquartered in the United States. The company’s location is relevant for understanding its regulatory framework and market focus, particularly in regions where U.S.-based manufacturers operate.
Which regulatory registries list Danmic Global, LLC’s devices?
The Aesthesio, Danmic Global, LLC’s primary device, is listed in the eudamed registry, which is the European Union’s central database for medical devices. This inclusion indicates compliance with EU Medical Device Regulations, ensuring traceability and transparency for authorized devices within the EU market.
How are Danmic Global, LLC’s devices classified under medical device regulations?
The Aesthesio is classified as a Class I medical device. This classification is typically assigned to low-risk devices, such as simple tools or devices with minimal risk to patient safety. The classification determines regulatory requirements, with Class I devices generally requiring less stringent oversight than higher-risk categories.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United States
- Address
- 2059, Camden Avenue #281, San Jose, United States
- Website
- www.danmicglobal.com/
- —
- —
- [email protected]
- Phone
- +1 408 626 0153
- PRRC Contact
- Dany Jensen
- EUDAMED SRN
- US-MF-000021060
- FDA FEI Number
- 3007602302
- DUNS Number
- —
Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Aesthesio | 514013 | EUDAMED | Class I | Active |
| Aesthesio | 514015 | EUDAMED | Class I | Active |
| Aesthesio | 514000-20C | EUDAMED | Class I | Active |
| Aesthesio | 514014 | EUDAMED | Class I | Active |
| Aesthesio | 514006 | EUDAMED | Class I | Active |
| Aesthesio | 514017 | EUDAMED | Class I | Active |
| Aesthesio | 514004 | EUDAMED | Class I | Active |
| Aesthesio | 514007 | EUDAMED | Class I | Active |
| Aesthesio | 514000-5C | EUDAMED | Class I | Active |
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