SU-KO TECHNOLOGIES LLC

FDA Device Registration & Listing · Austin, TX, US · Registration 3035372180

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
3035372180
FEI Number
3035372180
Entity Name
SU-KO TECHNOLOGIES LLC
City/State/Country
Austin, TX, US
Establishment Address
7801 N Lamar Blvd Ste F34, Austin, TX 78752, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Su-Ko Technologies LLC (Owner Number: 10092391)
Owner / Operator Contact Address
7801 N Lamar Blvd,, Suite F34, Austin, TX 78752, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K253153
PMA Number
N/A

All Registered Proprietary Names

SER Pen Carain Microsystem (MP1209SP) mdpen MD Pen

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QAI Powered Microneedle Device General, Plastic Surgery Class 2 878.4430 2025-05-16
QAI Powered Microneedle Device General, Plastic Surgery Class 2 878.4430 2026-03-12

Official Correspondent

Yuan Yuan Korrodi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Su-Ko Technologies LLC
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 3035372180. Last updated year: 2026. Please use registration number 3035372180 when referencing this establishment in official correspondence.
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