Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007602302

FEI Number

3007602302

Entity Name

DANMIC GLOBAL, LLC

City/State/Country

SAN JOSE, CA, US

Establishment Address

2059 CAMDEN AVE # 281, SAN JOSE, CA 95124, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Danmic Global, LLC (Owner Number: 10029364)

Owner / Operator Contact Address

1300 White Oaks Road, Suite 211, Campbell, CA 95008, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

AESTHESIO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GXB	Esthesiometer	Neurology	Class 1	882.1500	2012-10-13

Official Correspondent

Jorgen Jensen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Danmic Global, LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3004893971	MEDIPIN at JHS	Ware Hertfordshire, GB
2432177	FABRICATION ENT., INC.	ELMSFORD, NY, US
3012494290	SANICURE BV	SCHIPHOL Noord-Holland, NL
3011497622	GUANGZHOU GOLDSUN ELECTRONIC CO. LTD	Guangzhou Guangdong, CN
3001124136	INNOPEX LIMITED	Toronto Ontario, CA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007602302. Last updated year: 2026. Please use registration number 3007602302 when referencing this establishment in official correspondence.