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Danmic 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
LinkedIn
—
Facebook
—
Phone
+1 408 626 0153
PRRC Contact
Dany Jensen
EUDAMED SRN
US-MF-000021060
FDA FEI Number
3007602302
DUNS Number
—

Catalogue (9)

DeviceModel / ReferenceRegistriesClassStatus
Aesthesio 514013
EUDAMED
Class IActive
Aesthesio 514015
EUDAMED
Class IActive
Aesthesio 514000-20C
EUDAMED
Class IActive
Aesthesio 514014
EUDAMED
Class IActive
Aesthesio 514006
EUDAMED
Class IActive
Aesthesio 514017
EUDAMED
Class IActive
Aesthesio 514004
EUDAMED
Class IActive
Aesthesio 514007
EUDAMED
Class IActive
Aesthesio 514000-5C
EUDAMED
Class IActive

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