MINDERA CORPORATION

FDA Device Registration & Listing · Vista, CA, US · Registration 3016215282

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
3016215282
FEI Number
3016215282
Entity Name
MINDERA CORPORATION
City/State/Country
Vista, CA, US
Establishment Address
1221 Liberty Way, Vista, CA 92081, US
Establishment Type(s)
Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Mindera Corporation (Owner Number: 10075509)
Owner / Operator Contact Address
1221 Liberty Way, Vista, CA 92081, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mind.Px

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDD Kit, Surgical Instrument, Disposable General, Plastic Surgery Class 1 878.4800 2020-06-17

Official Correspondent

Byung-In Lee

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mindera Corporation
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 3016215282. Last updated year: 2026. Please use registration number 3016215282 when referencing this establishment in official correspondence.
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