FLEXTECH, INC.

FDA Device Registration & Listing · Saint Louis Park, MN, US · Registration 3008501679

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
3008501679
FEI Number
3008501679
Entity Name
FLEXTECH, INC.
City/State/Country
Saint Louis Park, MN, US
Establishment Address
7300 West 27th Street, Saint Louis Park, MN 55426, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Flextech, Inc. (Owner Number: 10083585)
Owner / Operator Contact Address
7300 West 27th Street, Saint Louis Park, MN 55426, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SecureMove-TLC

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PUK Administration Set Securement Device General Hospital Class 1 880.5210 2021-12-03

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Flextech, 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 3008501679. Last updated year: 2026. Please use registration number 3008501679 when referencing this establishment in official correspondence.
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