CLINICAL RESOLUTION LABORATORY, INC.

FDA Device Registration & Listing · Brea, CA, US · Registration 3005727243

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
3005727243
FEI Number
3005727243
Entity Name
CLINICAL RESOLUTION LABORATORY, INC.
City/State/Country
Brea, CA, US
Establishment Address
1530 Moonstone, Brea, CA 92821, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
CLINICAL RESOLUTION LABORATORY, INC. (Owner Number: 9086328)
Owner / Operator Contact Address
1530 Moonstone, Brea, CA 92821, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Innopen System Kit (Innopen & Innotip) MTS ROLLER MR2, MR3, MR5, MR10, MR15, MR20

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QQF Skin Microneedling Manual/Automated Device (Export Only) Unknown Class N N/A 2021-10-04

Official Correspondent

JUSTIN LEE

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CLINICAL RESOLUTION LABORATORY, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005727243. Last updated year: 2026. Please use registration number 3005727243 when referencing this establishment in official correspondence.
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