DYNAFLEX TECHNOLOGIES

FDA Device Registration & Listing · Irvine, CA, US · Registration 3013341368

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
3013341368
FEI Number
3013341368
Entity Name
DYNAFLEX TECHNOLOGIES
City/State/Country
Irvine, CA, US
Establishment Address
9 Goddard, Irvine, CA 92618, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Dynaflex Technologies (Owner Number: 10053287)
Owner / Operator Contact Address
22865 Savi Ranch Parkway, Suite F/G, Yorba Linda, CA 92887, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Not Applicable

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PTL Wire, Guide, Catheter, Exempt Cardiovascular Class 2 870.1330 2017-10-18

Official Correspondent

Shanshan Lin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dynaflex Technologies
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 3013341368. Last updated year: 2026. Please use registration number 3013341368 when referencing this establishment in official correspondence.
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