MIRIDIA TECHNOLOGY INC.

FDA Device Registration & Listing · Meridian, ID, US · Registration 3005356488

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005356488
FEI Number
3005356488
Entity Name
MIRIDIA TECHNOLOGY INC.
City/State/Country
Meridian, ID, US
Establishment Address
1875 N Lakes Pl, Meridian, ID 83646, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Miridia Technology Inc. (Owner Number: 10043867)
Owner / Operator Contact Address
1875 N. Lakes Place, Meridian, ID 83646, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AcuCore M1

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BWJ Locator, Acupuncture Point General Hospital Class 2 880.5580 2026-06-11

Official Correspondent

Adrian Larsen

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Miridia Technology Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005356488. Last updated year: 2026. Please use registration number 3005356488 when referencing this establishment in official correspondence.
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